Original source

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

T/-|Ancestral: T|MAF: 0.02 (T)

Chromosome 15:43063719 (forward strand)|View in location tab

Co-located variant

dbSNP rs199666034 (T/C)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57951808, rs56351870

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2513 sample genotypes.

Variant displays