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rs77493670

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs77493670(A;G)
Make rs77493670(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10287311
GeneICAM4
is asnp
is mentioned by
dbSNPrs77493670
ebirs77493670
HLIrs77493670
Exacrs77493670
Varsomers77493670
Maprs77493670
PheGenIrs77493670
hapmaprs77493670
1000 genomesrs77493670
hgdprs77493670
ensemblrs77493670
gopubmedrs77493670
geneviewrs77493670
scholarrs77493670
googlers77493670
pharmgkbrs77493670
gwascentralrs77493670
openSNPrs77493670
23andMers77493670
23andMe allrs77493670
SNP Nexus

SNPshotrs77493670
SNPdbers77493670
MSV3drs77493670
GWAS Ctlgrs77493670
GMAF0.001837
Max Magnitude0
OMIM111250
Desc
Variant0001
Relatedalso
ClinVar
Risk rs77493670(G;G)
Alt rs77493670(G;G)
Reference rs77493670(A;A)
Significance Other
Disease Landsteiner-Wiener phenotype
Variation info
Gene ICAM4
CLNDBN Landsteiner-Wiener phenotype
Reversed 0
HGVS NC_000019.9:g.10397987A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024094.3,