rs587778776

Orientation

plus

Stabilized

plus

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

Make rs587778776(A;A)

Make rs587778776(A;T)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

1804396

Gene

FGFR3

is a	snp
is	mentioned by
dbSNP	rs587778776
dbSNP (classic)	rs587778776
ClinGen	rs587778776
ebi	rs587778776
HLI	rs587778776
Exac	rs587778776
Gnomad	rs587778776
Varsome	rs587778776
LitVar	rs587778776
Map	rs587778776
PheGenI	rs587778776
Biobank	rs587778776
1000 genomes	rs587778776
hgdp	rs587778776
ensembl	rs587778776
geneview	rs587778776
scholar	rs587778776
google	rs587778776
pharmgkb	rs587778776
gwascentral	rs587778776
openSNP	rs587778776
23andMe	rs587778776
SNPshot	rs587778776
SNPdbe	rs587778776
MSV3d	rs587778776
GWAS Ctlg	rs587778776

Max Magnitude

0

ClinVar
Risk	rs587778776(A;A)
Alt	rs587778776(A;A)
Reference	Rs587778776(T;T)
Significance	Pathogenic
Disease	Hypochondroplasia
Variation	info
Gene	FGFR3
CLNDBN	Hypochondroplasia
Reversed	0
HGVS	NC_000004.11:g.1806123T>A
CLNSRC
CLNACC	RCV000056069.1,