Original source

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

Alleles
T/C/G|Ancestral: G|Ambiguity code: B|MAF: 0.23 (T)
Location

Chromosome 6:161515785 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs118125375, rs60603650

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2672 sample genotypes.

Variant displays