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rs137853214

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853214(G;T)
Make rs137853214(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position87349304
GeneRASA1
is asnp
is mentioned by
dbSNPrs137853214
ebirs137853214
HLIrs137853214
Exacrs137853214
Varsomers137853214
Maprs137853214
PheGenIrs137853214
hapmaprs137853214
1000 genomesrs137853214
hgdprs137853214
ensemblrs137853214
gopubmedrs137853214
geneviewrs137853214
scholarrs137853214
googlers137853214
pharmgkbrs137853214
gwascentralrs137853214
openSNPrs137853214
23andMers137853214
23andMe allrs137853214
SNP Nexus

SNPshotrs137853214
SNPdbers137853214
MSV3drs137853214
GWAS Ctlgrs137853214
Merged fromRs28932771
Max Magnitude0
OMIM139150
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853214(T;T)
Alt rs137853214(T;T)
Reference rs137853214(G;G)
Significance Pathogenic
Disease Basal cell carcinoma
Variation info
Gene RASA1
CLNDBN Basal cell carcinoma, somatic
Reversed 0
HGVS NC_000005.9:g.86645121G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000017367.4,