Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518215

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518215(A;A)
Make rs1057518215(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position28614686
GeneWAC
is asnp
is mentioned by
dbSNPrs1057518215
dbSNP (old)rs1057518215
ClinGenrs1057518215
ebirs1057518215
HLIrs1057518215
Exacrs1057518215
Gnomadrs1057518215
Varsomers1057518215
Maprs1057518215
PheGenIrs1057518215
Biobankrs1057518215
1000 genomesrs1057518215
hgdprs1057518215
ensemblrs1057518215
gopubmedrs1057518215
geneviewrs1057518215
scholarrs1057518215
googlers1057518215
pharmgkbrs1057518215
gwascentralrs1057518215
openSNPrs1057518215
23andMers1057518215
23andMe allrs1057518215
SNPshotrs1057518215
SNPdbers1057518215
MSV3drs1057518215
GWAS Ctlgrs1057518215
Max Magnitude0
ClinVar
Risk rs1057518215(A;A)
Alt rs1057518215(A;A)
Reference Rs1057518215(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WAC
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.28903615G>A
CLNSRC
CLNACC RCV000413536.1,