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rs886041234

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome9
Position35657804
GeneCCDC107, RMRP
is asnp
is mentioned by
dbSNPrs886041234
dbSNP (classic)rs886041234
ClinGenrs886041234
ebirs886041234
HLIrs886041234
Exacrs886041234
Gnomadrs886041234
Varsomers886041234
LitVarrs886041234
Maprs886041234
PheGenIrs886041234
Biobankrs886041234
1000 genomesrs886041234
hgdprs886041234
ensemblrs886041234
geneviewrs886041234
scholarrs886041234
googlers886041234
pharmgkbrs886041234
gwascentralrs886041234
openSNPrs886041234
23andMers886041234
SNPshotrs886041234
SNPdbers886041234
MSV3drs886041234
GWAS Ctlgrs886041234
Max Magnitude0
ClinVar
Risk rs886041234(C;C)
Alt rs886041234(C;C)
Reference Rs886041234(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene CCDC107 RMRP
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.35657801T>G
CLNSRC
CLNACC RCV000370918.1,