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rs28377268

From SNPedia

Orientationplus
Make rs28377268(G;G)
Make rs28377268(G;T)
Make rs28377268(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95462774
GeneLOC100507346, PTCH1
is asnp
is mentioned by
dbSNPrs28377268
ebirs28377268
HLIrs28377268
Exacrs28377268
Varsomers28377268
Maprs28377268
PheGenIrs28377268
hapmaprs28377268
1000 genomesrs28377268
hgdprs28377268
ensemblrs28377268
gopubmedrs28377268
geneviewrs28377268
scholarrs28377268
googlers28377268
pharmgkbrs28377268
gwascentralrs28377268
openSNPrs28377268
23andMers28377268
23andMe allrs28377268
SNP Nexus

SNPshotrs28377268
SNPdbers28377268
MSV3drs28377268
GWAS Ctlgrs28377268
Max Magnitude

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