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rs376177973

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376177973(G;T)
Make rs376177973(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140697311
GeneHARS2, ZMAT2
is asnp
is mentioned by
dbSNPrs376177973
ebirs376177973
HLIrs376177973
Exacrs376177973
Varsomers376177973
Maprs376177973
PheGenIrs376177973
hapmaprs376177973
1000 genomesrs376177973
hgdprs376177973
ensemblrs376177973
gopubmedrs376177973
geneviewrs376177973
scholarrs376177973
googlers376177973
pharmgkbrs376177973
gwascentralrs376177973
openSNPrs376177973
23andMers376177973
23andMe allrs376177973
SNP Nexus

SNPshotrs376177973
SNPdbers376177973
MSV3drs376177973
GWAS Ctlgrs376177973
Max Magnitude0
ClinVar
Risk rs376177973(A,T;A,T)
Alt rs376177973(A,T;A,T)
Reference rs376177973(G;G)
Significance Probable-Pathogenic
Disease Perrault syndrome 2
Variation info
Gene HARS2 ZMAT2
CLNDBN Perrault syndrome 2
Reversed 0
HGVS NC_000005.9:g.140076896G>T
CLNSRC
CLNACC RCV000206915.1,