Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

-/T | MAF: 0.48 (T)

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

Most severe consequence
Evidence status


Archive dbSNP rs138243832, rs59085181

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 1098 individual genotypes.

Variation displays