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rs121913529

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913529(C;C)
Make rs121913529(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position25245350
GeneKRAS
is asnp
is mentioned by
dbSNPrs121913529
ebirs121913529
HLIrs121913529
Exacrs121913529
Varsomers121913529
Maprs121913529
PheGenIrs121913529
hapmaprs121913529
1000 genomesrs121913529
hgdprs121913529
ensemblrs121913529
gopubmedrs121913529
geneviewrs121913529
scholarrs121913529
googlers121913529
pharmgkbrs121913529
gwascentralrs121913529
openSNPrs121913529
23andMers121913529
23andMe allrs121913529
SNP Nexus

SNPshotrs121913529
SNPdbers121913529
MSV3drs121913529
GWAS Ctlgrs121913529
Max Magnitude0
OMIM190070
Desc
Variant0005
Relatedalso
OMIM190070
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913529(A,C,T;A,C,T)
Alt rs121913529(A,C,T;A,C,T)
Reference rs121913529(G;G)
Significance Pathogenic
Disease Carcinoma of pancreas Nevus sebaceous Juvenile myelomonocytic leukemia Non-small cell lung cancer not provided Neoplasm of stomach Epidermal nevus Epidermal nevus syndrome RAS-associated autoimmune leukoproliferative disorder Neoplasm of ovary
Variation info
Gene KRAS
CLNDBN Carcinoma of pancreas Nevus sebaceous Juvenile myelomonocytic leukemia Non-small cell lung cancer not provided Neoplasm of stomach Epidermal nevus Epidermal nevus syndrome RAS-associated autoimmune leukoproliferative disorder Neoplasm of ovary
Reversed 1
HGVS NC_000012.11:g.25398284C>A; NC_000012.11:g.25398284C>G; NC_000012.11:g.25398284C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013413.4, RCV000029216.4, RCV000150895.1, RCV000154262.1, RCV000157944.2, RCV000038266.2, RCV000013411.5, RCV000013412.5, RCV000022799.5, RCV000029214.5, RCV000029215.5, RCV000144969.5, RCV000144970.3, RCV000150896.2, RCV000150897.2,