Original source

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

Alleles
G/- | Ancestral: G | MAF: < 0.01 (G)
Location

Chromosome 11:47462838 (forward strand) | View in location tab

Co-located

with dbSNP rs184381165 (G/A)

Most severe consequence
Evidence status

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

Variation displays