Original source

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

-/T | MAF: 0.48 (-)

Chromosome 11: between 102597994 and 102597995 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs138243832, rs59085181

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2510 sample genotypes.

Variant displays