Original source

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

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

Chromosome 6:10402388 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs2763175

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and has 1 sample genotype.

Variant displays