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rs201392711

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs201392711(A;G)
Make rs201392711(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140693654
GeneHARS, HARS2
is asnp
is mentioned by
dbSNPrs201392711
ebirs201392711
HLIrs201392711
Exacrs201392711
Varsomers201392711
Maprs201392711
PheGenIrs201392711
hapmaprs201392711
1000 genomesrs201392711
hgdprs201392711
ensemblrs201392711
gopubmedrs201392711
geneviewrs201392711
scholarrs201392711
googlers201392711
pharmgkbrs201392711
gwascentralrs201392711
openSNPrs201392711
23andMers201392711
23andMe allrs201392711
SNP Nexus

SNPshotrs201392711
SNPdbers201392711
MSV3drs201392711
GWAS Ctlgrs201392711
Max Magnitude0
ClinVar
Risk rs201392711(G;G)
Alt rs201392711(G;G)
Reference rs201392711(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HARS HARS2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.140073239A>G
CLNSRC
CLNACC RCV000197397.1,