Original source

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

C/- | Ancestral: C | MAF: 0.13 (-)

Chromosome 4:155210311 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs141933156

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2505 sample genotypes.

Variant displays