Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205590

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205590(C;G)
Make rs786205590(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position74360198
GeneGDAP1
is asnp
is mentioned by
dbSNPrs786205590
ebirs786205590
HLIrs786205590
Exacrs786205590
Varsomers786205590
Maprs786205590
PheGenIrs786205590
hapmaprs786205590
1000 genomesrs786205590
hgdprs786205590
ensemblrs786205590
gopubmedrs786205590
geneviewrs786205590
scholarrs786205590
googlers786205590
pharmgkbrs786205590
gwascentralrs786205590
openSNPrs786205590
23andMers786205590
23andMe allrs786205590
SNP Nexus

SNPshotrs786205590
SNPdbers786205590
MSV3drs786205590
GWAS Ctlgrs786205590
Max Magnitude0
ClinVar
Risk rs786205590(G;G)
Alt rs786205590(G;G)
Reference rs786205590(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GDAP1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.75272433C>G
CLNSRC
CLNACC RCV000171415.1,