Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.08 (T)
Location

Chromosome 10:69401215 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3750794

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2508 sample genotypes.

Variant displays