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

rs786205591

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205591(C;T)
Make rs786205591(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position74360257
GeneGDAP1
is asnp
is mentioned by
dbSNPrs786205591
ebirs786205591
HLIrs786205591
Exacrs786205591
Varsomers786205591
Maprs786205591
PheGenIrs786205591
hapmaprs786205591
1000 genomesrs786205591
hgdprs786205591
ensemblrs786205591
gopubmedrs786205591
geneviewrs786205591
scholarrs786205591
googlers786205591
pharmgkbrs786205591
gwascentralrs786205591
openSNPrs786205591
23andMers786205591
23andMe allrs786205591
SNP Nexus

SNPshotrs786205591
SNPdbers786205591
MSV3drs786205591
GWAS Ctlgrs786205591
Max Magnitude0
ClinVar
Risk rs786205591(T;T)
Alt rs786205591(T;T)
Reference rs786205591(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GDAP1
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.75272492C>T
CLNSRC
CLNACC RCV000171416.1,