Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.31 (T)
Location

Chromosome 10:31399087 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs4268416

HGVS names

This variant has 25 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2507 sample genotypes.

Variant displays