rs34003473

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rs34003473 has not been reported to ClinVar. Refer to dbSNP record rs34003473 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar

Genetic variation

Clinical significance: not reported in ClinVar
Reference allele: TTTTTTTTTTTTTTT
Variation alleles: TTTTTT, TTTTTTT, TTTTTTTTTT
Variation type: insertion/deletion

Organism: Homo sapiens
GRCh38.p14: NC_000010.11: 87,960,876
GRCh37.p13: NC_000010.10: 89,720,633

Genome Data Viewer

Search results

Items: 7

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 802611	NM_000314.8(PTEN):c.802-5_802-3dup	PTEN	Duplication (intron variant)	Breast and/or ovarian cancer +4 more	GBenign/Likely benign
Select item 92832	NM_000314.8(PTEN):c.802-4_802-3dup	PTEN	Duplication (intron variant)	Glioma susceptibility 2 +7 more	GBenign/Likely benign
Select item 92831	NM_000314.8(PTEN):c.802-3dup	PTEN	Duplication (intron variant)	Malignant tumor of prostate +8 more	GBenign
Select item 1529483	NM_000314.8(PTEN):c.802-11_802-3del	PTEN	Deletion (intron variant)	PTEN hamartoma tumor syndrome	GLikely benign
Select item 229656	NM_000314.8(PTEN):c.802-5_802-3del	PTEN	Deletion (intron variant)	Breast and/or ovarian cancer +2 more	GConflicting classifications of pathogenicity
Select item 229653	NM_000314.8(PTEN):c.802-3del	PTEN	Deletion (intron variant)	not specified +4 more	GBenign/Likely benign
Select item 92833	NM_000314.8(PTEN):c.802-4_802-3del	PTEN	Deletion (intron variant)	Breast and/or ovarian cancer +2 more	GBenign/Likely benign

ClinVar

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Genetic variation

rs34003473

Search results

Items: 7