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rs104894191

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894191(C;T)
Make rs104894191(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position44309645
GeneALX4
is asnp
is mentioned by
dbSNPrs104894191
ebirs104894191
HLIrs104894191
Exacrs104894191
Varsomers104894191
Maprs104894191
PheGenIrs104894191
hapmaprs104894191
1000 genomesrs104894191
hgdprs104894191
ensemblrs104894191
gopubmedrs104894191
geneviewrs104894191
scholarrs104894191
googlers104894191
pharmgkbrs104894191
gwascentralrs104894191
openSNPrs104894191
23andMers104894191
23andMe allrs104894191
SNP Nexus

SNPshotrs104894191
SNPdbers104894191
MSV3drs104894191
GWAS Ctlgrs104894191
Max Magnitude0
OMIM605420
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894191(T;T)
Alt rs104894191(T;T)
Reference rs104894191(C;C)
Significance Pathogenic
Disease Parietal foramina 2
Variation info
Gene ALX4
CLNDBN Parietal foramina 2
Reversed 1
HGVS NC_000011.9:g.44331195G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005316.4,