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rs727502904

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727502904(A;A)
Make rs727502904(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position140734763
GeneBRAF
is asnp
is mentioned by
dbSNPrs727502904
ebirs727502904
HLIrs727502904
Exacrs727502904
Varsomers727502904
Maprs727502904
PheGenIrs727502904
hapmaprs727502904
1000 genomesrs727502904
hgdprs727502904
ensemblrs727502904
gopubmedrs727502904
geneviewrs727502904
scholarrs727502904
googlers727502904
pharmgkbrs727502904
gwascentralrs727502904
openSNPrs727502904
23andMers727502904
23andMe allrs727502904
SNP Nexus

SNPshotrs727502904
SNPdbers727502904
MSV3drs727502904
GWAS Ctlgrs727502904
Max Magnitude0
ClinVar
Risk rs727502904(A;A)
Alt rs727502904(A;A)
Reference rs727502904(C;C)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene BRAF
CLNDBN Rasopathy
Reversed 1
HGVS NC_000007.13:g.140434563G>T
CLNSRC
CLNACC RCV000150197.2,