Original source

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

T/C/G | Ambiguity code: B | MAF: 0.18 (T)

Chromosome 5:162106919 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs117115163

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2505 sample genotypes.

Variant displays