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rs104894364

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894364(C;T)
Make rs104894364(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25227351
GeneKRAS
is asnp
is mentioned by
dbSNPrs104894364
ebirs104894364
HLIrs104894364
Exacrs104894364
Varsomers104894364
Maprs104894364
PheGenIrs104894364
hapmaprs104894364
1000 genomesrs104894364
hgdprs104894364
ensemblrs104894364
gopubmedrs104894364
geneviewrs104894364
scholarrs104894364
googlers104894364
pharmgkbrs104894364
gwascentralrs104894364
openSNPrs104894364
23andMers104894364
23andMe allrs104894364
SNP Nexus

SNPshotrs104894364
SNPdbers104894364
MSV3drs104894364
GWAS Ctlgrs104894364
Max Magnitude0
OMIM190070
Desc
Variant0011
Relatedalso
ClinVar
Risk rs104894364(T;T)
Alt rs104894364(T;T)
Reference rs104894364(C;C)
Significance Pathogenic
Disease Noonan syndrome 3 not provided Noonan syndrome
Variation info
Gene KRAS
CLNDBN Noonan syndrome 3 not provided Noonan syndrome
Reversed 1
HGVS NC_000012.11:g.25380285G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000013419.20, RCV000157933.1, RCV000211785.1,