Original source

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

G/A|Ancestral: A|Ambiguity code: R|MAF: 0.45 (G)

Chromosome 8:93919644 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs61297781

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanHap550, Illumina_HumanHap650Y

About this variant

This variant overlaps 12 transcripts and has 3673 sample genotypes.

Variant displays