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rs1057518124

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518124(G;G)
Make rs1057518124(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position37784965
GeneEXOSC3
is asnp
is mentioned by
dbSNPrs1057518124
dbSNP (old)rs1057518124
ClinGenrs1057518124
ebirs1057518124
HLIrs1057518124
Exacrs1057518124
Gnomadrs1057518124
Varsomers1057518124
Maprs1057518124
PheGenIrs1057518124
Biobankrs1057518124
1000 genomesrs1057518124
hgdprs1057518124
ensemblrs1057518124
gopubmedrs1057518124
geneviewrs1057518124
scholarrs1057518124
googlers1057518124
pharmgkbrs1057518124
gwascentralrs1057518124
openSNPrs1057518124
23andMers1057518124
23andMe allrs1057518124
SNPshotrs1057518124
SNPdbers1057518124
MSV3drs1057518124
GWAS Ctlgrs1057518124
Max Magnitude0
ClinVar
Risk rs1057518124(G;G)
Alt rs1057518124(G;G)
Reference Rs1057518124(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene EXOSC3
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.37784962A>C
CLNSRC
CLNACC RCV000414156.1,