rs2277439

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs2277439(A;A)

Make rs2277439(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

42581307

Gene

TNFSF11

is a	snp
is	mentioned by
dbSNP	rs2277439
dbSNP (classic)	rs2277439
ClinGen	rs2277439
ebi	rs2277439
HLI	rs2277439
Exac	rs2277439
Gnomad	rs2277439
Varsome	rs2277439
LitVar	rs2277439
Map	rs2277439
PheGenI	rs2277439
Biobank	rs2277439
1000 genomes	rs2277439
hgdp	rs2277439
ensembl	rs2277439
geneview	rs2277439
scholar	rs2277439
google	rs2277439
pharmgkb	rs2277439
gwascentral	rs2277439
openSNP	rs2277439
23andMe	rs2277439
SNPshot	rs2277439
SNPdbe	rs2277439
MSV3d	rs2277439
GWAS Ctlg	rs2277439

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[PMID 25138264] Polymorphisms in genes in the RANKL/RANK/OPG pathway are associated with bone mineral density at different skeletal sites in post-menopausal women

ClinVar
Risk	rs2277439(A;A)
Alt	rs2277439(A;A)
Reference	Rs2277439(G;G)
Significance	Non-pathogenic
Disease	not specified Osteopetrosis
Variation	info
Gene	TNFSF11
CLNDBN	not specified Osteopetrosis
Reversed	0
HGVS	NC_000013.10:g.43155443G>A
CLNSRC
CLNACC	RCV000175758.1, RCV000400844.1,