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rs140540222

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs140540222(C;T)
Make rs140540222(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140695556
GeneHARS2
is asnp
is mentioned by
dbSNPrs140540222
ebirs140540222
HLIrs140540222
Exacrs140540222
Varsomers140540222
Maprs140540222
PheGenIrs140540222
hapmaprs140540222
1000 genomesrs140540222
hgdprs140540222
ensemblrs140540222
gopubmedrs140540222
geneviewrs140540222
scholarrs140540222
googlers140540222
pharmgkbrs140540222
gwascentralrs140540222
openSNPrs140540222
23andMers140540222
23andMe allrs140540222
SNP Nexus

SNPshotrs140540222
SNPdbers140540222
MSV3drs140540222
GWAS Ctlgrs140540222
Max Magnitude0
ClinVar
Risk rs140540222(T;T)
Alt rs140540222(T;T)
Reference rs140540222(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene HARS2
CLNDBN not provided not specified
Reversed 0
HGVS NC_000005.9:g.140075141C>T
CLNSRC
CLNACC RCV000199285.1, RCV000223531.1,