Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.47 (T)
Location

Chromosome 6:161531855 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59792638, rs56629917

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 7 transcripts and has 3960 sample genotypes.

Variant displays