Original source

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

T/- | Ancestral: T | MAF: 0.17 (-)

Chromosome 4:120706086 (forward strand) | View in location tab


with dbSNP rs75046371 (T/C)

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2505 sample genotypes.

Variant displays