Have questions? Visit https://www.reddit.com/r/SNPedia

rs137853216

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853216(A;G)
Make rs137853216(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position87349312
GeneRASA1
is asnp
is mentioned by
dbSNPrs137853216
ebirs137853216
HLIrs137853216
Exacrs137853216
Varsomers137853216
Maprs137853216
PheGenIrs137853216
hapmaprs137853216
1000 genomesrs137853216
hgdprs137853216
ensemblrs137853216
gopubmedrs137853216
geneviewrs137853216
scholarrs137853216
googlers137853216
pharmgkbrs137853216
gwascentralrs137853216
openSNPrs137853216
23andMers137853216
23andMe allrs137853216
SNP Nexus

SNPshotrs137853216
SNPdbers137853216
MSV3drs137853216
GWAS Ctlgrs137853216
Merged fromRs28932772
Max Magnitude0
OMIM139150
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853216(G;G)
Alt rs137853216(G;G)
Reference rs137853216(A;A)
Significance Pathogenic
Disease Basal cell carcinoma
Variation info
Gene RASA1
CLNDBN Basal cell carcinoma, somatic
Reversed 0
HGVS NC_000005.9:g.86645129A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000017369.4,