Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.34 (C)
Location

Chromosome 11:60852184 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR042843

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1224037, rs57414459

This variation has 2 HGVS names - click the plus to show

11:g.60852184T>C
ENST00000332539.4:c.*351A>G

Variation displays