Original source

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

G/C | Ambiguity code: S

Chromosome 6:10399922 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs2857056

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2 sample genotypes.

Variant displays