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rs786205442

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205442(A;A)
Make rs786205442(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position32786971
GeneYARS
is asnp
is mentioned by
dbSNPrs786205442
ebirs786205442
HLIrs786205442
Exacrs786205442
Varsomers786205442
Maprs786205442
PheGenIrs786205442
hapmaprs786205442
1000 genomesrs786205442
hgdprs786205442
ensemblrs786205442
gopubmedrs786205442
geneviewrs786205442
scholarrs786205442
googlers786205442
pharmgkbrs786205442
gwascentralrs786205442
openSNPrs786205442
23andMers786205442
23andMe allrs786205442
SNP Nexus

SNPshotrs786205442
SNPdbers786205442
MSV3drs786205442
GWAS Ctlgrs786205442
Max Magnitude0
ClinVar
Risk rs786205442(A;A)
Alt rs786205442(A;A)
Reference rs786205442(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene YARS
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.33252572G>T
CLNSRC
CLNACC RCV000171150.1,