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rs137853217

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853217(A;A)
Make rs137853217(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position87369821
GeneRASA1
is asnp
is mentioned by
dbSNPrs137853217
ebirs137853217
HLIrs137853217
Exacrs137853217
Varsomers137853217
Maprs137853217
PheGenIrs137853217
hapmaprs137853217
1000 genomesrs137853217
hgdprs137853217
ensemblrs137853217
gopubmedrs137853217
geneviewrs137853217
scholarrs137853217
googlers137853217
pharmgkbrs137853217
gwascentralrs137853217
openSNPrs137853217
23andMers137853217
23andMe allrs137853217
SNP Nexus

SNPshotrs137853217
SNPdbers137853217
MSV3drs137853217
GWAS Ctlgrs137853217
Max Magnitude0
OMIM139150
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853217(A;A)
Alt rs137853217(A;A)
Reference rs137853217(G;G)
Significance Pathogenic
Disease Capillary malformation-arteriovenous malformation
Variation info
Gene RASA1
CLNDBN Capillary malformation-arteriovenous malformation
Reversed 0
HGVS NC_000005.9:g.86665638G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017372.27,