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rs1060503439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs1060503439(-;-)
Make rs1060503439(-;CA)
Make rs1060503439(CA;CA)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position87362576
GeneCCNH, RASA1
is asnp
is mentioned by
dbSNPrs1060503439
dbSNP (old)rs1060503439
ClinGenrs1060503439
ebirs1060503439
HLIrs1060503439
Exacrs1060503439
Gnomadrs1060503439
Varsomers1060503439
LitVarrs1060503439
Maprs1060503439
PheGenIrs1060503439
Biobankrs1060503439
1000 genomesrs1060503439
hgdprs1060503439
ensemblrs1060503439
gopubmedrs1060503439
geneviewrs1060503439
scholarrs1060503439
googlers1060503439
pharmgkbrs1060503439
gwascentralrs1060503439
openSNPrs1060503439
23andMers1060503439
23andMe allrs1060503439
SNPshotrs1060503439
SNPdbers1060503439
MSV3drs1060503439
GWAS Ctlgrs1060503439
Max Magnitude0
ClinVar
Risk rs1060503439(-;-)
Alt rs1060503439(-;-)
Reference Rs1060503439(AC;AC)
Significance Pathogenic
Disease Capillary malformation-arteriovenous malformation
Variation info
Gene RASA1
CLNDBN Capillary malformation-arteriovenous malformation
Reversed 0
HGVS NC_000005.9:g.86658393_86658394delCA
CLNSRC
CLNACC RCV000473537.1,