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rs202219398

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202219398(A;A)
Make rs202219398(A;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position130133373
GeneAIFM1
is asnp
is mentioned by
dbSNPrs202219398
ebirs202219398
HLIrs202219398
Exacrs202219398
Varsomers202219398
Maprs202219398
PheGenIrs202219398
hapmaprs202219398
1000 genomesrs202219398
hgdprs202219398
ensemblrs202219398
gopubmedrs202219398
geneviewrs202219398
scholarrs202219398
googlers202219398
pharmgkbrs202219398
gwascentralrs202219398
openSNPrs202219398
23andMers202219398
23andMe allrs202219398
SNP Nexus

SNPshotrs202219398
SNPdbers202219398
MSV3drs202219398
GWAS Ctlgrs202219398
Max Magnitude0
ClinVar
Risk rs202219398(A;A)
Alt rs202219398(A;A)
Reference rs202219398(C;C)
Significance Probable-Pathogenic
Disease Cowchock syndrome
Variation info
Gene AIFM1
CLNDBN Cowchock syndrome
Reversed 0
HGVS NC_000023.10:g.129267348C>A
CLNSRC
CLNACC RCV000235074.1,