Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 11:6636673 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990373

Most severe consequence
Evidence status

Clinical significance

Synonyms

Uniprot VAR_009610

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

Variation displays