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rs727505017

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727505017(C;C)
Make rs727505017(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12604201
GeneRAF1
is asnp
is mentioned by
dbSNPrs727505017
ebirs727505017
HLIrs727505017
Exacrs727505017
Varsomers727505017
Maprs727505017
PheGenIrs727505017
hapmaprs727505017
1000 genomesrs727505017
hgdprs727505017
ensemblrs727505017
gopubmedrs727505017
geneviewrs727505017
scholarrs727505017
googlers727505017
pharmgkbrs727505017
gwascentralrs727505017
openSNPrs727505017
23andMers727505017
23andMe allrs727505017
SNP Nexus

SNPshotrs727505017
SNPdbers727505017
MSV3drs727505017
GWAS Ctlgrs727505017
Max Magnitude0
ClinVar
Risk rs727505017(C;C)
Alt rs727505017(C;C)
Reference rs727505017(T;T)
Significance Pathogenic
Disease Noonan syndrome not provided Primary familial hypertrophic cardiomyopathy
Variation info
Gene RAF1
CLNDBN Noonan syndrome not provided Primary familial hypertrophic cardiomyopathy
Reversed 1
HGVS NC_000003.11:g.12645700A>G
CLNSRC
CLNACC RCV000156441.2, RCV000159073.1, RCV000208439.1,