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rs62620995

From SNPedia

Orientationplus
Stabilizedplus
Make rs62620995(C;C)
Make rs62620995(C;T)
Make rs62620995(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position104355036
GeneDCSTAMP
is asnp
is mentioned by
dbSNPrs62620995
ebirs62620995
HLIrs62620995
Exacrs62620995
Varsomers62620995
Maprs62620995
PheGenIrs62620995
hapmaprs62620995
1000 genomesrs62620995
hgdprs62620995
ensemblrs62620995
gopubmedrs62620995
geneviewrs62620995
scholarrs62620995
googlers62620995
pharmgkbrs62620995
gwascentralrs62620995
openSNPrs62620995
23andMers62620995
23andMe allrs62620995
SNP Nexus

SNPshotrs62620995
SNPdbers62620995
MSV3drs62620995
GWAS Ctlgrs62620995
GMAF0.005969
Max Magnitude

[PMID 24370779] Identification of rare genetic variants in novel loci associated with Paget's disease of bone