Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503384

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503384(C;G)
Make rs727503384(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position12611985
GeneRAF1
is asnp
is mentioned by
dbSNPrs727503384
ebirs727503384
HLIrs727503384
Exacrs727503384
Varsomers727503384
Maprs727503384
PheGenIrs727503384
hapmaprs727503384
1000 genomesrs727503384
hgdprs727503384
ensemblrs727503384
gopubmedrs727503384
geneviewrs727503384
scholarrs727503384
googlers727503384
pharmgkbrs727503384
gwascentralrs727503384
openSNPrs727503384
23andMers727503384
23andMe allrs727503384
SNP Nexus

SNPshotrs727503384
SNPdbers727503384
MSV3drs727503384
GWAS Ctlgrs727503384
Max Magnitude0
ClinVar
Risk rs727503384(G;G)
Alt rs727503384(G;G)
Reference rs727503384(C;C)
Significance Probable-Pathogenic
Disease Noonan syndrome
Variation info
Gene RAF1
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000003.11:g.12653484G>C
CLNSRC
CLNACC RCV000151719.1,