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rs727504370

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504370(A;G)
Make rs727504370(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position4110558
GeneMAP2K2
is asnp
is mentioned by
dbSNPrs727504370
ebirs727504370
HLIrs727504370
Exacrs727504370
Varsomers727504370
Maprs727504370
PheGenIrs727504370
hapmaprs727504370
1000 genomesrs727504370
hgdprs727504370
ensemblrs727504370
gopubmedrs727504370
geneviewrs727504370
scholarrs727504370
googlers727504370
pharmgkbrs727504370
gwascentralrs727504370
openSNPrs727504370
23andMers727504370
23andMe allrs727504370
SNP Nexus

SNPshotrs727504370
SNPdbers727504370
MSV3drs727504370
GWAS Ctlgrs727504370
Max Magnitude0
ClinVar
Risk rs727504370(G;G)
Alt rs727504370(G;G)
Reference rs727504370(A;A)
Significance Pathogenic
Disease Rasopathy Cardiofaciocutaneous syndrome
Variation info
Gene MAP2K2
CLNDBN Rasopathy Cardiofaciocutaneous syndrome
Reversed 1
HGVS NC_000019.9:g.4110556T>C
CLNSRC
CLNACC RCV000154507.1, RCV000208747.1,