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rs774528745

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774528745(C;T)
Make rs774528745(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position222221368
GeneLOC105373901, LOC107985991, PAX3
is asnp
is mentioned by
dbSNPrs774528745
dbSNP (classic)rs774528745
ClinGenrs774528745
ebirs774528745
HLIrs774528745
Exacrs774528745
Gnomadrs774528745
Varsomers774528745
LitVarrs774528745
Maprs774528745
PheGenIrs774528745
Biobankrs774528745
1000 genomesrs774528745
hgdprs774528745
ensemblrs774528745
geneviewrs774528745
scholarrs774528745
googlers774528745
pharmgkbrs774528745
gwascentralrs774528745
openSNPrs774528745
23andMers774528745
SNPshotrs774528745
SNPdbers774528745
MSV3drs774528745
GWAS Ctlgrs774528745
Max Magnitude0
ClinVar
Risk rs774528745(T;T)
Alt rs774528745(T;T)
Reference Rs774528745(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PAX3
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.223086087C>T
CLNSRC
CLNACC RCV000372931.1,