Original source

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

C/- | Ancestral: C | MAF: 0.03 (-)

Chromosome 1:12168975 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs377529180, rs140748620

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 1136 individual genotypes.

Variation displays