Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.13 (G)
Location

Chromosome 17:76137021 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs16968584

This variation has 2 HGVS names - click the plus to show

17:g.76137021C>G
ENST00000322957.6:c.*332G>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2509 individual genotypes.

Variation displays