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rs7955866

From SNPedia

Orientationplus
Stabilizedplus
Make rs7955866(A;A)
Make rs7955866(A;G)
Make rs7955866(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position4370383
GeneFGF23
is asnp
is mentioned by
dbSNPrs7955866
ebirs7955866
HLIrs7955866
Exacrs7955866
Varsomers7955866
Maprs7955866
PheGenIrs7955866
hapmaprs7955866
1000 genomesrs7955866
hgdprs7955866
ensemblrs7955866
gopubmedrs7955866
geneviewrs7955866
scholarrs7955866
googlers7955866
pharmgkbrs7955866
gwascentralrs7955866
openSNPrs7955866
23andMers7955866
23andMe allrs7955866
SNP Nexus

SNPshotrs7955866
SNPdbers7955866
MSV3drs7955866
GWAS Ctlgrs7955866
GMAF0.1382
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 20394945] Infantile hypercalcemia and hypercalciuria: new insights into a vitamin D-dependent mechanism and response to ketoconazole treatment


[PMID 22419710] A Functional Allelic Variant of the FGF23 Gene Is Associated with Renal Phosphate Leak in Calcium Nephrolithiasis


GET Evidence
FGF23-T239M
aa_change Thr239Met
aa_change_short T239M
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.104852
summary



[PMID 25445451] FGF23 gene variation and its association with phosphate homeostasis and bone mineral density in Finnish children and adolescents