Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 8:118933071 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM034979

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 11321, 2010_April_001_062_TNFRSF11B_602643_0003

This variation has 5 HGVS names - click the plus to show

Variation displays