Original source

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

T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.36 (C)

Chromosome 5:159323005 (forward strand)|View in location tab

Co-located variant

dbSNP rs747937531 (T/-)

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 4 transcripts, has 2977 sample genotypes and is mentioned in 8 citations.

Variant displays