Original source

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

-/T | MAF: 0.04 (T)

Chromosome 12: between 43757179 and 43757180 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs370140457, rs369543384

This variation has 10 HGVS names - click the plus to show

About this variant

This variant overlaps 21 transcripts and has 1092 individual genotypes.

Variation displays