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rs72658152

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72658152(A;A)
Make rs72658152(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position94418508
GeneCOL1A2
is asnp
is mentioned by
dbSNPrs72658152
dbSNP (classic)rs72658152
ClinGenrs72658152
ebirs72658152
HLIrs72658152
Exacrs72658152
Gnomadrs72658152
Varsomers72658152
LitVarrs72658152
Maprs72658152
PheGenIrs72658152
Biobankrs72658152
1000 genomesrs72658152
hgdprs72658152
ensemblrs72658152
geneviewrs72658152
scholarrs72658152
googlers72658152
pharmgkbrs72658152
gwascentralrs72658152
openSNPrs72658152
23andMers72658152
SNPshotrs72658152
SNPdbers72658152
MSV3drs72658152
GWAS Ctlgrs72658152
Max Magnitude0
OMIM120160
Desc
Variant0030
Relatedalso


ClinVar
Risk rs72658152(A;A)
Alt rs72658152(A;A)
Reference Rs72658152(G;G)
Significance Pathogenic
Disease Postmenopausal osteoporosis
Variation info
Gene COL1A2
CLNDBN Postmenopausal osteoporosis
Reversed 0
HGVS NC_000007.13:g.94047820G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018799.28,