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rs104894196

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894196(C;C)
Make rs104894196(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position44267585
GeneALX4
is asnp
is mentioned by
dbSNPrs104894196
ebirs104894196
HLIrs104894196
Exacrs104894196
Varsomers104894196
Maprs104894196
PheGenIrs104894196
hapmaprs104894196
1000 genomesrs104894196
hgdprs104894196
ensemblrs104894196
gopubmedrs104894196
geneviewrs104894196
scholarrs104894196
googlers104894196
pharmgkbrs104894196
gwascentralrs104894196
openSNPrs104894196
23andMers104894196
23andMe allrs104894196
SNP Nexus

SNPshotrs104894196
SNPdbers104894196
MSV3drs104894196
GWAS Ctlgrs104894196
Max Magnitude0
OMIM605420
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894196(C;C)
Alt rs104894196(C;C)
Reference rs104894196(G;G)
Significance Pathogenic
Disease Parietal foramina 2
Variation info
Gene ALX4
CLNDBN Parietal foramina 2
Reversed 1
HGVS NC_000011.9:g.44289135C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005320.4,