Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/- | Ancestral: T
Location

Chromosome 5:158742208 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71577370, rs376535119

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

Variation displays