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rs863223718

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223718(C;T)
Make rs863223718(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position87376512
GeneLOC105379067, RASA1
is asnp
is mentioned by
dbSNPrs863223718
ebirs863223718
HLIrs863223718
Exacrs863223718
Varsomers863223718
Maprs863223718
PheGenIrs863223718
hapmaprs863223718
1000 genomesrs863223718
hgdprs863223718
ensemblrs863223718
gopubmedrs863223718
geneviewrs863223718
scholarrs863223718
googlers863223718
pharmgkbrs863223718
gwascentralrs863223718
openSNPrs863223718
23andMers863223718
23andMe allrs863223718
SNP Nexus

SNPshotrs863223718
SNPdbers863223718
MSV3drs863223718
GWAS Ctlgrs863223718
Max Magnitude0
ClinVar
Risk rs863223718(T;T)
Alt rs863223718(T;T)
Reference rs863223718(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RASA1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.86672329C>T
CLNSRC
CLNACC RCV000196439.2,