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rs4975596

From SNPedia

Orientationminus
Stabilizedminus
Make rs4975596(A;A)
Make rs4975596(A;G)
Make rs4975596(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position1189232
is asnp
is mentioned by
dbSNPrs4975596
ebirs4975596
HLIrs4975596
Exacrs4975596
Varsomers4975596
Maprs4975596
PheGenIrs4975596
hapmaprs4975596
1000 genomesrs4975596
hgdprs4975596
ensemblrs4975596
gopubmedrs4975596
geneviewrs4975596
scholarrs4975596
googlers4975596
pharmgkbrs4975596
gwascentralrs4975596
openSNPrs4975596
23andMers4975596
23andMe allrs4975596
SNP Nexus

SNPshotrs4975596
SNPdbers4975596
MSV3drs4975596
GWAS Ctlgrs4975596
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 24152305OA-icon.png] Association of candidate single nucleotide polymorphisms with somatic mutation of the epidermal growth factor receptor pathway