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rs137853218

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853218(C;T)
Make rs137853218(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position87333291
GeneRASA1
is asnp
is mentioned by
dbSNPrs137853218
ebirs137853218
HLIrs137853218
Exacrs137853218
Varsomers137853218
Maprs137853218
PheGenIrs137853218
hapmaprs137853218
1000 genomesrs137853218
hgdprs137853218
ensemblrs137853218
gopubmedrs137853218
geneviewrs137853218
scholarrs137853218
googlers137853218
pharmgkbrs137853218
gwascentralrs137853218
openSNPrs137853218
23andMers137853218
23andMe allrs137853218
SNP Nexus

SNPshotrs137853218
SNPdbers137853218
MSV3drs137853218
GWAS Ctlgrs137853218
Max Magnitude0
OMIM139150
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137853218(T;T)
Alt rs137853218(T;T)
Reference rs137853218(C;C)
Significance Pathogenic
Disease Capillary malformation without arteriovenous malformation
Variation info
Gene RASA1
CLNDBN Capillary malformation without arteriovenous malformation
Reversed 0
HGVS NC_000005.9:g.86629108C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017373.27,