rs11063112

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs11063112(A;A)

Make rs11063112(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

4368914

Gene

FGF23

is a	snp
is	mentioned by
dbSNP	rs11063112
dbSNP (classic)	rs11063112
ClinGen	rs11063112
ebi	rs11063112
HLI	rs11063112
Exac	rs11063112
Gnomad	rs11063112
Varsome	rs11063112
LitVar	rs11063112
Map	rs11063112
PheGenI	rs11063112
Biobank	rs11063112
1000 genomes	rs11063112
hgdp	rs11063112
ensembl	rs11063112
geneview	rs11063112
scholar	rs11063112
google	rs11063112
pharmgkb	rs11063112
gwascentral	rs11063112
openSNP	rs11063112
23andMe	rs11063112
SNPshot	rs11063112
SNPdbe	rs11063112
MSV3d	rs11063112
GWAS Ctlg	rs11063112

Max Magnitude

0

?	(A;A) (A;T) (T;T)	28

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

ClinVar
Risk	rs11063112(A;A)
Alt	rs11063112(A;A)
Reference	Rs11063112(T;T)
Significance	Non-pathogenic
Disease	Hypophosphatemic Rickets Tumoral calcinosis
Variation	info
Gene	FGF23
CLNDBN	Hypophosphatemic Rickets, Dominant Tumoral calcinosis, familial, hyperphosphatemic
Reversed	0
HGVS	NC_000012.11:g.4478080T>A
CLNSRC
CLNACC	RCV000297238.1, RCV000356756.1,