Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.31 (A)
Location

Chromosome 1:115829313 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM086294

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays