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rs774909609

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774909609(C;T)
Make rs774909609(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position34990673
GeneDNAJB5, DNAJB5-AS1
is asnp
is mentioned by
dbSNPrs774909609
ebirs774909609
HLIrs774909609
Exacrs774909609
Varsomers774909609
Maprs774909609
PheGenIrs774909609
hapmaprs774909609
1000 genomesrs774909609
hgdprs774909609
ensemblrs774909609
gopubmedrs774909609
geneviewrs774909609
scholarrs774909609
googlers774909609
pharmgkbrs774909609
gwascentralrs774909609
openSNPrs774909609
23andMers774909609
23andMe allrs774909609
SNP Nexus

SNPshotrs774909609
SNPdbers774909609
MSV3drs774909609
GWAS Ctlgrs774909609
Max Magnitude0
ClinVar
Risk rs774909609(T;T)
Alt rs774909609(T;T)
Reference rs774909609(C;C)
Significance Probable-Pathogenic
Disease Peripheral neuropathy Skeletal myopathy
Variation info
Gene DNAJB5-AS1 LOC101926900 DNAJB5
CLNDBN Peripheral neuropathy Skeletal myopathy
Reversed 0
HGVS NC_000009.11:g.34990670C>T
CLNSRC
CLNACC RCV000235050.1,