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rs878854569

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878854569(-;-)
Make rs878854569(-;T)
Make rs878854569(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position87379776
GeneRASA1
is asnp
is mentioned by
dbSNPrs878854569
ebirs878854569
HLIrs878854569
Exacrs878854569
Varsomers878854569
Maprs878854569
PheGenIrs878854569
hapmaprs878854569
1000 genomesrs878854569
hgdprs878854569
ensemblrs878854569
gopubmedrs878854569
geneviewrs878854569
scholarrs878854569
googlers878854569
pharmgkbrs878854569
gwascentralrs878854569
openSNPrs878854569
23andMers878854569
23andMe allrs878854569
SNP Nexus

SNPshotrs878854569
SNPdbers878854569
MSV3drs878854569
GWAS Ctlgrs878854569
Max Magnitude0
ClinVar
Risk rs878854569(T;T)
Alt rs878854569(T;T)
Reference rs878854569(;)
Significance Pathogenic
Disease Capillary malformation-arteriovenous malformation
Variation info
Gene RASA1
CLNDBN Capillary malformation-arteriovenous malformation
Reversed 0
HGVS NC_000005.9:g.86675593dupT
CLNSRC
CLNACC RCV000232710.1,