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

rs864309503

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309503(C;T)
Make rs864309503(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position30941503
GeneMORC2
is asnp
is mentioned by
dbSNPrs864309503
ebirs864309503
HLIrs864309503
Exacrs864309503
Varsomers864309503
Maprs864309503
PheGenIrs864309503
hapmaprs864309503
1000 genomesrs864309503
hgdprs864309503
ensemblrs864309503
gopubmedrs864309503
geneviewrs864309503
scholarrs864309503
googlers864309503
pharmgkbrs864309503
gwascentralrs864309503
openSNPrs864309503
23andMers864309503
23andMe allrs864309503
SNP Nexus

SNPshotrs864309503
SNPdbers864309503
MSV3drs864309503
GWAS Ctlgrs864309503
Max Magnitude0
ClinVar
Risk rs864309503(T;T)
Alt rs864309503(T;T)
Reference rs864309503(C;C)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene MORC2
CLNDBN Charcot-Marie-Tooth disease, axonal, type 2z
Reversed 1
HGVS NC_000022.10:g.31337490G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000202547.2,