| Resource Links | Submitted Gene Name | RET | Submitted Gene ID | N.D. | Submitted SNP Synonyms | N.D | Submitted linkout | N.D | Submitted HGVS | NM_020975.4:c.2712C>G |
| Assay | Species | Homo sapiens | Molecular Type | genomic | Method | CLINICAL_SNP_SUBMISSION | Ascertainment Samplesize | N.D. | Population | N.D. |
| Allele | Observed Allele | C/G | Ancestral Allele | N.D. | Allele Origin | G:Germline C:Germline | SNP Class | SNV | CpG Code | N.D. |
| | Variation | Frequency Submission | N.D. | Genotype Summary | N.D. | Genotype Submission | N.D. | Haplotype | N.D. |
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>gnl|dbSNP|ss749736347|allelePos=51|len=101|taxid=9606|alleles='C/G'|mol=Genomic ATGAAGATTT CGGATTTCGG CTTGTCCCGA GATGTTTATG AAGAGGATTC
S
TACGTGAAGA GGAGCCAGGT GCCCAGTCCC GGGGATGAGG CGGGGCTCCC
There is no frequency submission for ss749736347.
No sufficient data to compute Hardy-weinberg probability for ss749736347.
There is no individual genotype data for ss749736347.
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