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rs1085307765

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position35657871
GeneCCDC107, RMRP
is asnp
is mentioned by
dbSNPrs1085307765
dbSNP (classic)rs1085307765
ClinGenrs1085307765
ebirs1085307765
HLIrs1085307765
Exacrs1085307765
Gnomadrs1085307765
Varsomers1085307765
LitVarrs1085307765
Maprs1085307765
PheGenIrs1085307765
Biobankrs1085307765
1000 genomesrs1085307765
hgdprs1085307765
ensemblrs1085307765
geneviewrs1085307765
scholarrs1085307765
googlers1085307765
pharmgkbrs1085307765
gwascentralrs1085307765
openSNPrs1085307765
23andMers1085307765
23andMe allrs1085307765
SNPshotrs1085307765
SNPdbers1085307765
MSV3drs1085307765
GWAS Ctlgrs1085307765
Max Magnitude0
ClinVar
Risk rs1085307765(T;T)
Alt rs1085307765(T;T)
Reference Rs1085307765(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CCDC107 RMRP
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.35657868G>A
CLNSRC
CLNACC RCV000490106.1,