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rs376618

From SNPedia

Orientationminus
Stabilizedminus
Make rs376618(A;A)
Make rs376618(A;G)
Make rs376618(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position177090796
GeneFGFR4
is asnp
is mentioned by
dbSNPrs376618
ebirs376618
HLIrs376618
Exacrs376618
Varsomers376618
Maprs376618
PheGenIrs376618
hapmaprs376618
1000 genomesrs376618
hgdprs376618
ensemblrs376618
gopubmedrs376618
geneviewrs376618
scholarrs376618
googlers376618
pharmgkbrs376618
gwascentralrs376618
openSNPrs376618
23andMers376618
23andMe allrs376618
SNP Nexus

SNPshotrs376618
SNPdbers376618
MSV3drs376618
GWAS Ctlgrs376618
GMAF0.185
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21656577] Association between fibroblast growth factor receptor 4 polymorphisms and risk of hepatocellular carcinoma


[PMID 18762813OA-icon.png] Association of FGFR4 genetic polymorphisms with prostate cancer risk and prognosis.


[PMID 19500394OA-icon.png] Genetic variants in FGFR2 and FGFR4 genes and skin cancer risk in the Nurses' Health Study.


GET Evidence
FGFR4-P136L
aa_change Pro136Leu
aa_change_short P136L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.721974
summary