Original source

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

T/- | Ancestral: T

Chromosome 5:159315200 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs71577370, rs376535119

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 4 individual genotypes.

Variation displays