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rs137853215

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853215(A;G)
Make rs137853215(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position87349309
GeneRASA1
is asnp
is mentioned by
dbSNPrs137853215
ebirs137853215
HLIrs137853215
Exacrs137853215
Varsomers137853215
Maprs137853215
PheGenIrs137853215
hapmaprs137853215
1000 genomesrs137853215
hgdprs137853215
ensemblrs137853215
gopubmedrs137853215
geneviewrs137853215
scholarrs137853215
googlers137853215
pharmgkbrs137853215
gwascentralrs137853215
openSNPrs137853215
23andMers137853215
23andMe allrs137853215
SNP Nexus

SNPshotrs137853215
SNPdbers137853215
MSV3drs137853215
GWAS Ctlgrs137853215
Max Magnitude0
OMIM139150
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853215(G;G)
Alt rs137853215(G;G)
Reference rs137853215(A;A)
Significance Pathogenic
Disease Basal cell carcinoma
Variation info
Gene RASA1
CLNDBN Basal cell carcinoma, somatic
Reversed 0
HGVS NC_000005.9:g.86645126A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017368.4,