Original source

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

Alleles
T/G|Ancestral: G|Ambiguity code: K|MAF: 0.28 (T)
Location

Chromosome 8:39926138 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs59976974

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2509 sample genotypes.

Variant displays