Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: < 0.01 (G)
Location

Chromosome 11:108135240 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM014309

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15249

This variation has 9 HGVS names - click the plus to show

Variation displays