Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/C | Ancestral: G | Ambiguity code: S

Chromosome 17:63917902 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_011918

HGVS names

This variant has 11 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_Human660W-quad

About this variant

This variant overlaps 7 transcripts and has 267 sample genotypes.

Variant displays