Original source

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

Alleles
C/A | Ambiguity code: M | MAF: 0.27 (A)
Location

Chromosome 10:135346927 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57034966

This variation has 8 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

Variation displays