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rs770501034

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770501034(C;T)
Make rs770501034(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position74364059
GeneGDAP1
is asnp
is mentioned by
dbSNPrs770501034
ebirs770501034
HLIrs770501034
Exacrs770501034
Varsomers770501034
Maprs770501034
PheGenIrs770501034
hapmaprs770501034
1000 genomesrs770501034
hgdprs770501034
ensemblrs770501034
gopubmedrs770501034
geneviewrs770501034
scholarrs770501034
googlers770501034
pharmgkbrs770501034
gwascentralrs770501034
openSNPrs770501034
23andMers770501034
23andMe allrs770501034
SNP Nexus

SNPshotrs770501034
SNPdbers770501034
MSV3drs770501034
GWAS Ctlgrs770501034
Max Magnitude0
ClinVar
Risk rs770501034(T;T)
Alt rs770501034(T;T)
Reference rs770501034(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GDAP1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.75276294C>T
CLNSRC
CLNACC RCV000235362.1,