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rs727504375

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504375(A;C)
Make rs727504375(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position140778059
GeneBRAF
is asnp
is mentioned by
dbSNPrs727504375
ebirs727504375
HLIrs727504375
Exacrs727504375
Varsomers727504375
Maprs727504375
PheGenIrs727504375
hapmaprs727504375
1000 genomesrs727504375
hgdprs727504375
ensemblrs727504375
gopubmedrs727504375
geneviewrs727504375
scholarrs727504375
googlers727504375
pharmgkbrs727504375
gwascentralrs727504375
openSNPrs727504375
23andMers727504375
23andMe allrs727504375
SNP Nexus

SNPshotrs727504375
SNPdbers727504375
MSV3drs727504375
GWAS Ctlgrs727504375
Max Magnitude0
ClinVar
Risk rs727504375(C;C)
Alt rs727504375(C;C)
Reference rs727504375(A;A)
Significance Probable-Pathogenic
Disease Rasopathy
Variation info
Gene BRAF
CLNDBN Rasopathy
Reversed 1
HGVS NC_000007.13:g.140477859T>G
CLNSRC
CLNACC RCV000154526.1,