Original source

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

-/G | MAF: 0.47 (G)

Chromosome 11: between 102598048 and 102598049 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs149118200, rs56736408

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

About this variant

This variant overlaps 3 transcripts and has 1098 individual genotypes.

Variation displays