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rs1064793373

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position35657968
GeneCCDC107, RMRP
is asnp
is mentioned by
dbSNPrs1064793373
dbSNP (old)rs1064793373
ClinGenrs1064793373
ebirs1064793373
HLIrs1064793373
Exacrs1064793373
Gnomadrs1064793373
Varsomers1064793373
Maprs1064793373
PheGenIrs1064793373
Biobankrs1064793373
1000 genomesrs1064793373
hgdprs1064793373
ensemblrs1064793373
gopubmedrs1064793373
geneviewrs1064793373
scholarrs1064793373
googlers1064793373
pharmgkbrs1064793373
gwascentralrs1064793373
openSNPrs1064793373
23andMers1064793373
23andMe allrs1064793373
SNPshotrs1064793373
SNPdbers1064793373
MSV3drs1064793373
GWAS Ctlgrs1064793373
Max Magnitude0
ClinVar
Risk rs1064793373(T;T)
Alt rs1064793373(T;T)
Reference Rs1064793373(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CCDC107 RMRP
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.35657965G>A
CLNSRC
CLNACC RCV000487375.1,