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rs3730271

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3730271(C;C)
Make rs3730271(C;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position12604195
GeneRAF1
is asnp
is mentioned by
dbSNPrs3730271
ebirs3730271
HLIrs3730271
Exacrs3730271
Varsomers3730271
Maprs3730271
PheGenIrs3730271
hapmaprs3730271
1000 genomesrs3730271
hgdprs3730271
ensemblrs3730271
gopubmedrs3730271
geneviewrs3730271
scholarrs3730271
googlers3730271
pharmgkbrs3730271
gwascentralrs3730271
openSNPrs3730271
23andMers3730271
23andMe allrs3730271
SNP Nexus

SNPshotrs3730271
SNPdbers3730271
MSV3drs3730271
GWAS Ctlgrs3730271
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs3730271(A,C;A,C)
Alt rs3730271(A,C;A,C)
Reference rs3730271(T;T)
Significance Pathogenic
Disease Noonan syndrome not provided
Variation info
Gene RAF1
CLNDBN Noonan syndrome not provided
Reversed 1
HGVS NC_000003.11:g.12645694A>G; NC_000003.11:g.12645694A>T
CLNSRC ClinVar
CLNACC RCV000215259.1, RCV000037698.2, RCV000159074.2,