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rs398122410

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs398122410(A;A)
Make rs398122410(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position169769610
GeneERMARD
is asnp
is mentioned by
dbSNPrs398122410
ebirs398122410
HLIrs398122410
Exacrs398122410
Varsomers398122410
Maprs398122410
PheGenIrs398122410
hapmaprs398122410
1000 genomesrs398122410
hgdprs398122410
ensemblrs398122410
gopubmedrs398122410
geneviewrs398122410
scholarrs398122410
googlers398122410
pharmgkbrs398122410
gwascentralrs398122410
openSNPrs398122410
23andMers398122410
23andMe allrs398122410
SNP Nexus

SNPshotrs398122410
SNPdbers398122410
MSV3drs398122410
GWAS Ctlgrs398122410
Max Magnitude0
ClinVar
Risk rs398122410(A;A)
Alt rs398122410(A;A)
Reference rs398122410(T;T)
Significance Pathogenic
Disease Periventricular nodular heterotopia 6
Variation info
Gene C6orf70 ERMARD
CLNDBN Periventricular nodular heterotopia 6
Reversed 0
HGVS NC_000006.11:g.170169706T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074458.5,