Original source

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

-/A | MAF: 0.26 (A)

Chromosome 12: between 21131687 and 21131688 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs374850048, rs140501804

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 1098 individual genotypes.

Variation displays