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rs577721086

From SNPedia

Orientationplus
Stabilizedplus
Make rs577721086(C;C)
Make rs577721086(C;T)
Make rs577721086(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position127118902
GeneLOC105377989, RSPO3
is asnp
is mentioned by
dbSNPrs577721086
dbSNP (old)rs577721086
ClinGenrs577721086
ebirs577721086
HLIrs577721086
Exacrs577721086
Varsomers577721086
Maprs577721086
PheGenIrs577721086
Biobankrs577721086
1000 genomesrs577721086
hgdprs577721086
ensemblrs577721086
gopubmedrs577721086
geneviewrs577721086
scholarrs577721086
googlers577721086
pharmgkbrs577721086
gwascentralrs577721086
openSNPrs577721086
23andMers577721086
23andMe allrs577721086
SNP Nexus

SNPshotrs577721086
SNPdbers577721086
MSV3drs577721086
GWAS Ctlgrs577721086
Max Magnitude

[PMID 26733130OA-icon.png] Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.