Original source

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

-/A | MAF: 0.34 (A)

Chromosome 1: between 236797951 and 236797952 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs145816061, rs145201177

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

About this variant

This variant overlaps 3 transcripts and has 1096 individual genotypes.

Variation displays