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rs12775980

From SNPedia

Orientationplus
Stabilizedplus
Make rs12775980(A;A)
Make rs12775980(A;C)
Make rs12775980(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position29570927
GeneSVIL
is asnp
is mentioned by
dbSNPrs12775980
dbSNP (classic)rs12775980
ClinGenrs12775980
ebirs12775980
HLIrs12775980
Exacrs12775980
Gnomadrs12775980
Varsomers12775980
LitVarrs12775980
Maprs12775980
PheGenIrs12775980
Biobankrs12775980
1000 genomesrs12775980
hgdprs12775980
ensemblrs12775980
geneviewrs12775980
scholarrs12775980
googlers12775980
pharmgkbrs12775980
gwascentralrs12775980
openSNPrs12775980
23andMers12775980
23andMe allrs12775980
SNPshotrs12775980
SNPdbers12775980
MSV3drs12775980
GWAS Ctlgrs12775980
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 28580392OA-icon.png] A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women.