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rs757576534

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757576534(A;A)
Make rs757576534(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position35657873
GeneCCDC107, RMRP
is asnp
is mentioned by
dbSNPrs757576534
dbSNP (classic)rs757576534
ClinGenrs757576534
ebirs757576534
HLIrs757576534
Exacrs757576534
Gnomadrs757576534
Varsomers757576534
LitVarrs757576534
Maprs757576534
PheGenIrs757576534
Biobankrs757576534
1000 genomesrs757576534
hgdprs757576534
ensemblrs757576534
geneviewrs757576534
scholarrs757576534
googlers757576534
pharmgkbrs757576534
gwascentralrs757576534
openSNPrs757576534
23andMers757576534
SNPshotrs757576534
SNPdbers757576534
MSV3drs757576534
GWAS Ctlgrs757576534
Max Magnitude0
ClinVar
Risk rs757576534(A;A) rs757576534(T;T)
Alt rs757576534(A;A) rs757576534(T;T)
Reference Rs757576534(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CCDC107 RMRP
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.35657870G>A
CLNSRC
CLNACC RCV000423534.1,