Original source

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

AA/- | MAF: 0.01 (-)

Chromosome 7:101128962-101128963 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs376316305, rs201280512

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 1138 individual genotypes.

Variation displays