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rs139194636

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs139194636(C;C)
Make rs139194636(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position119033203
GeneWARS2
is asnp
is mentioned by
dbSNPrs139194636
ebirs139194636
HLIrs139194636
Exacrs139194636
Varsomers139194636
Maprs139194636
PheGenIrs139194636
hapmaprs139194636
1000 genomesrs139194636
hgdprs139194636
ensemblrs139194636
gopubmedrs139194636
geneviewrs139194636
scholarrs139194636
googlers139194636
pharmgkbrs139194636
gwascentralrs139194636
openSNPrs139194636
23andMers139194636
23andMe allrs139194636
SNP Nexus

SNPshotrs139194636
SNPdbers139194636
MSV3drs139194636
GWAS Ctlgrs139194636
Max Magnitude0
ClinVar
Risk rs139194636(C;C)
Alt rs139194636(C;C)
Reference rs139194636(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WARS2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.119575826T>C
CLNSRC
CLNACC RCV000209945.1,