Original source

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

G/A|Ambiguity code: R|MAF: 0.07 (G)

Chromosome 14:102138013 (forward strand)|View in location tab

Co-located variant

dbSNP rs201102946 (G/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs60866357, rs1742625

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2507 sample genotypes.

Variant displays