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rs759998394

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759998394(C;T)
Make rs759998394(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position151892356
GeneGLRA1
is asnp
is mentioned by
dbSNPrs759998394
dbSNP (classic)rs759998394
ClinGenrs759998394
ebirs759998394
HLIrs759998394
Exacrs759998394
Gnomadrs759998394
Varsomers759998394
LitVarrs759998394
Maprs759998394
PheGenIrs759998394
Biobankrs759998394
1000 genomesrs759998394
hgdprs759998394
ensemblrs759998394
geneviewrs759998394
scholarrs759998394
googlers759998394
pharmgkbrs759998394
gwascentralrs759998394
openSNPrs759998394
23andMers759998394
23andMe allrs759998394
SNPshotrs759998394
SNPdbers759998394
MSV3drs759998394
GWAS Ctlgrs759998394
Max Magnitude0
ClinVar
Risk rs759998394(T;T)
Alt rs759998394(T;T)
Reference Rs759998394(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GLRA1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.151271917C>T
CLNSRC
CLNACC RCV000493956.1,