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rs369634007

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs369634007(A;G)
Make rs369634007(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position112098688
GeneTMEM87B
is asnp
is mentioned by
dbSNPrs369634007
ebirs369634007
HLIrs369634007
Exacrs369634007
Varsomers369634007
Maprs369634007
PheGenIrs369634007
hapmaprs369634007
1000 genomesrs369634007
hgdprs369634007
ensemblrs369634007
gopubmedrs369634007
geneviewrs369634007
scholarrs369634007
googlers369634007
pharmgkbrs369634007
gwascentralrs369634007
openSNPrs369634007
23andMers369634007
23andMe allrs369634007
SNP Nexus

SNPshotrs369634007
SNPdbers369634007
MSV3drs369634007
GWAS Ctlgrs369634007
Max Magnitude0
ClinVar
Risk rs369634007(G;G)
Alt rs369634007(G;G)
Reference rs369634007(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TMEM87B
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.112856265A>G
CLNSRC
CLNACC RCV000208660.1,