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rs1060503440

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503440(C;T)
Make rs1060503440(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position87389522
GeneCCNH, RASA1
is asnp
is mentioned by
dbSNPrs1060503440
dbSNP (old)rs1060503440
ClinGenrs1060503440
ebirs1060503440
HLIrs1060503440
Exacrs1060503440
Gnomadrs1060503440
Varsomers1060503440
Maprs1060503440
PheGenIrs1060503440
Biobankrs1060503440
1000 genomesrs1060503440
hgdprs1060503440
ensemblrs1060503440
gopubmedrs1060503440
geneviewrs1060503440
scholarrs1060503440
googlers1060503440
pharmgkbrs1060503440
gwascentralrs1060503440
openSNPrs1060503440
23andMers1060503440
23andMe allrs1060503440
SNPshotrs1060503440
SNPdbers1060503440
MSV3drs1060503440
GWAS Ctlgrs1060503440
Max Magnitude0
ClinVar
Risk rs1060503440(T;T)
Alt rs1060503440(T;T)
Reference Rs1060503440(C;C)
Significance Probable-Pathogenic
Disease Capillary malformation-arteriovenous malformation
Variation info
Gene RASA1
CLNDBN Capillary malformation-arteriovenous malformation
Reversed 0
HGVS NC_000005.9:g.86685339C>T
CLNSRC
CLNACC RCV000459359.1,