Original source

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

A/C|Ancestral: C|Ambiguity code: M|MAF: 0.40 (A)

Chromosome 10:99533711 (forward strand)|View in location tab

Co-located variant

dbSNP rs200965740 (A/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60567633

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 3 transcripts and has 2511 sample genotypes.

Variant displays