Original source

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

Alleles
G/C|Ambiguity code: S
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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