rs587778816

Orientation

plus

Stabilized

plus

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

Make rs587778816(C;G)

Make rs587778816(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

1803731

Gene

FGFR3

is a	snp
is	mentioned by
dbSNP	rs587778816
dbSNP (classic)	rs587778816
ClinGen	rs587778816
ebi	rs587778816
HLI	rs587778816
Exac	rs587778816
Gnomad	rs587778816
Varsome	rs587778816
LitVar	rs587778816
Map	rs587778816
PheGenI	rs587778816
Biobank	rs587778816
1000 genomes	rs587778816
hgdp	rs587778816
ensembl	rs587778816
geneview	rs587778816
scholar	rs587778816
google	rs587778816
pharmgkb	rs587778816
gwascentral	rs587778816
openSNP	rs587778816
23andMe	rs587778816
SNPshot	rs587778816
SNPdbe	rs587778816
MSV3d	rs587778816
GWAS Ctlg	rs587778816

Max Magnitude

0

ClinVar
Risk	rs587778816(G;G)
Alt	rs587778816(G;G)
Reference	Rs587778816(C;C)
Significance	Pathogenic
Disease	Hypochondroplasia
Variation	info
Gene	FGFR3
CLNDBN	Hypochondroplasia
Reversed	0
HGVS	NC_000004.11:g.1805458C>G
CLNSRC
CLNACC	RCV000056161.1,