Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 11:113323370 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs71063506, rs376927423

This variation has 6 HGVS names - click the plus to show

Variation displays