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rs1057518233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518233(C;T)
Make rs1057518233(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position28608338
GeneWAC
is asnp
is mentioned by
dbSNPrs1057518233
dbSNP (old)rs1057518233
ClinGenrs1057518233
ebirs1057518233
HLIrs1057518233
Exacrs1057518233
Gnomadrs1057518233
Varsomers1057518233
Maprs1057518233
PheGenIrs1057518233
Biobankrs1057518233
1000 genomesrs1057518233
hgdprs1057518233
ensemblrs1057518233
gopubmedrs1057518233
geneviewrs1057518233
scholarrs1057518233
googlers1057518233
pharmgkbrs1057518233
gwascentralrs1057518233
openSNPrs1057518233
23andMers1057518233
23andMe allrs1057518233
SNPshotrs1057518233
SNPdbers1057518233
MSV3drs1057518233
GWAS Ctlgrs1057518233
Max Magnitude0
ClinVar
Risk rs1057518233(T;T)
Alt rs1057518233(T;T)
Reference Rs1057518233(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene WAC
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.28897267C>T
CLNSRC
CLNACC RCV000413960.1,