Original source

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

Alleles
G/C|Ancestral: C|Ambiguity code: S|MAF: 0.03 (G)
Location

Chromosome 12:11687255 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs862790, rs60068750, rs1210184

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2509 sample genotypes.

Variant displays