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rs1060503438

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060503438(A;A)
Make rs1060503438(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position87385390
GeneCCNH, RASA1
is asnp
is mentioned by
dbSNPrs1060503438
dbSNP (old)rs1060503438
ClinGenrs1060503438
ebirs1060503438
HLIrs1060503438
Exacrs1060503438
Gnomadrs1060503438
Varsomers1060503438
Maprs1060503438
PheGenIrs1060503438
Biobankrs1060503438
1000 genomesrs1060503438
hgdprs1060503438
ensemblrs1060503438
gopubmedrs1060503438
geneviewrs1060503438
scholarrs1060503438
googlers1060503438
pharmgkbrs1060503438
gwascentralrs1060503438
openSNPrs1060503438
23andMers1060503438
23andMe allrs1060503438
SNPshotrs1060503438
SNPdbers1060503438
MSV3drs1060503438
GWAS Ctlgrs1060503438
Max Magnitude0
ClinVar
Risk rs1060503438(A;A)
Alt rs1060503438(A;A)
Reference Rs1060503438(G;G)
Significance Probable-Pathogenic
Disease Capillary malformation-arteriovenous malformation
Variation info
Gene RASA1
CLNDBN Capillary malformation-arteriovenous malformation
Reversed 0
HGVS NC_000005.9:g.86681207G>A
CLNSRC
CLNACC RCV000457601.1,