Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with dbSNP rs75046371 (T/C)

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2505 individual genotypes.

Variation displays