Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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