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rs757600616

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs757600616(A;A)
Make rs757600616(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position119033279
GeneWARS2
is asnp
is mentioned by
dbSNPrs757600616
ebirs757600616
HLIrs757600616
Exacrs757600616
Varsomers757600616
Maprs757600616
PheGenIrs757600616
hapmaprs757600616
1000 genomesrs757600616
hgdprs757600616
ensemblrs757600616
gopubmedrs757600616
geneviewrs757600616
scholarrs757600616
googlers757600616
pharmgkbrs757600616
gwascentralrs757600616
openSNPrs757600616
23andMers757600616
23andMe allrs757600616
SNP Nexus

SNPshotrs757600616
SNPdbers757600616
MSV3drs757600616
GWAS Ctlgrs757600616
Max Magnitude0
ClinVar
Risk rs757600616(A;A)
Alt rs757600616(A;A)
Reference rs757600616(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WARS2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.119575902G>A
CLNSRC
CLNACC RCV000209871.1,