rs587778773

Orientation

plus

Stabilized

plus

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

Make rs587778773(C;T)

Make rs587778773(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

1801886

Gene

FGFR3

is a	snp
is	mentioned by
dbSNP	rs587778773
dbSNP (classic)	rs587778773
ClinGen	rs587778773
ebi	rs587778773
HLI	rs587778773
Exac	rs587778773
Gnomad	rs587778773
Varsome	rs587778773
LitVar	rs587778773
Map	rs587778773
PheGenI	rs587778773
Biobank	rs587778773
1000 genomes	rs587778773
hgdp	rs587778773
ensembl	rs587778773
geneview	rs587778773
scholar	rs587778773
google	rs587778773
pharmgkb	rs587778773
gwascentral	rs587778773
openSNP	rs587778773
23andMe	rs587778773
SNPshot	rs587778773
SNPdbe	rs587778773
MSV3d	rs587778773
GWAS Ctlg	rs587778773

Max Magnitude

0

ClinVar
Risk	rs587778773(T;T)
Alt	rs587778773(T;T)
Reference	Rs587778773(C;C)
Significance	Pathogenic
Disease	Hypochondroplasia
Variation	info
Gene	FGFR3
CLNDBN	Hypochondroplasia
Reversed	0
HGVS	NC_000004.11:g.1803613C>T
CLNSRC
CLNACC	RCV000056063.1,