Original source

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

T/C/G | Ancestral: T | Ambiguity code: B | MAF: < 0.01 (G)

Chromosome 4:174490141 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 24 transcripts and has 2504 sample genotypes.

Variant displays