Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: 0.43 (G)

Chromosome 5:139320954 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 29 transcripts and has 2510 sample genotypes.

Variant displays