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rs863224040

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224040(A;A)
Make rs863224040(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140695846
GeneHARS2
is asnp
is mentioned by
dbSNPrs863224040
ebirs863224040
HLIrs863224040
Exacrs863224040
Varsomers863224040
Maprs863224040
PheGenIrs863224040
hapmaprs863224040
1000 genomesrs863224040
hgdprs863224040
ensemblrs863224040
gopubmedrs863224040
geneviewrs863224040
scholarrs863224040
googlers863224040
pharmgkbrs863224040
gwascentralrs863224040
openSNPrs863224040
23andMers863224040
23andMe allrs863224040
SNP Nexus

SNPshotrs863224040
SNPdbers863224040
MSV3drs863224040
GWAS Ctlgrs863224040
Max Magnitude0
ClinVar
Risk rs863224040(A;A)
Alt rs863224040(A;A)
Reference rs863224040(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene HARS2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.140075431G>A
CLNSRC
CLNACC RCV000195718.1,