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rs727504662

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504662(A;T)
Make rs727504662(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position25227310
GeneKRAS
is asnp
is mentioned by
dbSNPrs727504662
ebirs727504662
HLIrs727504662
Exacrs727504662
Varsomers727504662
Maprs727504662
PheGenIrs727504662
hapmaprs727504662
1000 genomesrs727504662
hgdprs727504662
ensemblrs727504662
gopubmedrs727504662
geneviewrs727504662
scholarrs727504662
googlers727504662
pharmgkbrs727504662
gwascentralrs727504662
openSNPrs727504662
23andMers727504662
23andMe allrs727504662
SNP Nexus

SNPshotrs727504662
SNPdbers727504662
MSV3drs727504662
GWAS Ctlgrs727504662
Max Magnitude0
ClinVar
Risk rs727504662(T;T)
Alt rs727504662(T;T)
Reference rs727504662(A;A)
Significance Pathogenic
Disease Noonan syndrome
Variation info
Gene KRAS
CLNDBN Noonan syndrome
Reversed 1
HGVS NC_000012.11:g.25380244T>A
CLNSRC
CLNACC RCV000155926.2,