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rs104894197

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894197(A;A)
Make rs104894197(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position44275505
GeneALX4
is asnp
is mentioned by
dbSNPrs104894197
ebirs104894197
HLIrs104894197
Exacrs104894197
Varsomers104894197
Maprs104894197
PheGenIrs104894197
hapmaprs104894197
1000 genomesrs104894197
hgdprs104894197
ensemblrs104894197
gopubmedrs104894197
geneviewrs104894197
scholarrs104894197
googlers104894197
pharmgkbrs104894197
gwascentralrs104894197
openSNPrs104894197
23andMers104894197
23andMe allrs104894197
SNP Nexus

SNPshotrs104894197
SNPdbers104894197
MSV3drs104894197
GWAS Ctlgrs104894197
Max Magnitude0
OMIM605420
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894197(A,T;A,T)
Alt rs104894197(A,T;A,T)
Reference rs104894197(C;C)
Significance Pathogenic
Disease Parietal foramina 2
Variation info
Gene ALX4
CLNDBN Parietal foramina 2
Reversed 1
HGVS NC_000011.9:g.44297055G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005321.4,