Original source

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

CA/- | MAF: 0.02 (-)

Chromosome 2:237485600-237485601 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs373561649

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

About this variant

This variant overlaps 10 transcripts and has 1092 individual genotypes.

Variation displays