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rs863223719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223719(A;A)
Make rs863223719(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position87380596
GeneCCNH, RASA1
is asnp
is mentioned by
dbSNPrs863223719
dbSNP (classic)rs863223719
ClinGenrs863223719
ebirs863223719
HLIrs863223719
Exacrs863223719
Gnomadrs863223719
Varsomers863223719
LitVarrs863223719
Maprs863223719
PheGenIrs863223719
Biobankrs863223719
1000 genomesrs863223719
hgdprs863223719
ensemblrs863223719
geneviewrs863223719
scholarrs863223719
googlers863223719
pharmgkbrs863223719
gwascentralrs863223719
openSNPrs863223719
23andMers863223719
SNPshotrs863223719
SNPdbers863223719
MSV3drs863223719
GWAS Ctlgrs863223719
Max Magnitude0
ClinVar
Risk rs863223719(A;A)
Alt rs863223719(A;A)
Reference Rs863223719(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RASA1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.86676413G>A
CLNSRC
CLNACC RCV000197942.1,