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rs397516830

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Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397516830(G;G)
Make rs397516830(G;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position12604182
GeneRAF1
is asnp
is mentioned by
dbSNPrs397516830
ebirs397516830
HLIrs397516830
Exacrs397516830
Varsomers397516830
Maprs397516830
PheGenIrs397516830
hapmaprs397516830
1000 genomesrs397516830
hgdprs397516830
ensemblrs397516830
gopubmedrs397516830
geneviewrs397516830
scholarrs397516830
googlers397516830
pharmgkbrs397516830
gwascentralrs397516830
openSNPrs397516830
23andMers397516830
23andMe allrs397516830
SNP Nexus

SNPshotrs397516830
SNPdbers397516830
MSV3drs397516830
GWAS Ctlgrs397516830
Max Magnitude0
ClinVar
Risk rs397516830(G;G)
Alt rs397516830(G;G)
Reference rs397516830(T;T)
Significance Other
Disease Noonan syndrome not provided
Variation info
Gene RAF1
CLNDBN Noonan syndrome not provided
Reversed 1
HGVS NC_000003.11:g.12645681A>C
CLNSRC ClinVar
CLNACC RCV000037708.4, RCV000159078.1,