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rs104894192

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894192(C;T)
Make rs104894192(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position44275389
GeneALX4
is asnp
is mentioned by
dbSNPrs104894192
ebirs104894192
HLIrs104894192
Exacrs104894192
Varsomers104894192
Maprs104894192
PheGenIrs104894192
hapmaprs104894192
1000 genomesrs104894192
hgdprs104894192
ensemblrs104894192
gopubmedrs104894192
geneviewrs104894192
scholarrs104894192
googlers104894192
pharmgkbrs104894192
gwascentralrs104894192
openSNPrs104894192
23andMers104894192
23andMe allrs104894192
SNP Nexus

SNPshotrs104894192
SNPdbers104894192
MSV3drs104894192
GWAS Ctlgrs104894192
Max Magnitude0
OMIM605420
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894192(T;T)
Alt rs104894192(T;T)
Reference rs104894192(C;C)
Significance Pathogenic
Disease Parietal foramina 2
Variation info
Gene ALX4
CLNDBN Parietal foramina 2
Reversed 1
HGVS NC_000011.9:g.44296939G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005317.4,