Original source

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

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

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

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

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