rs121913115

Orientation

plus

Stabilized

plus

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

Make rs121913115(A;G)

Make rs121913115(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

1801928

Gene

FGFR3

is a	snp
is	mentioned by
dbSNP	rs121913115
dbSNP (classic)	rs121913115
ClinGen	rs121913115
ebi	rs121913115
HLI	rs121913115
Exac	rs121913115
Gnomad	rs121913115
Varsome	rs121913115
LitVar	rs121913115
Map	rs121913115
PheGenI	rs121913115
Biobank	rs121913115
1000 genomes	rs121913115
hgdp	rs121913115
ensembl	rs121913115
geneview	rs121913115
scholar	rs121913115
google	rs121913115
pharmgkb	rs121913115
gwascentral	rs121913115
openSNP	rs121913115
23andMe	rs121913115
SNPshot	rs121913115
SNPdbe	rs121913115
MSV3d	rs121913115
GWAS Ctlg	rs121913115

Max Magnitude

0

OMIM	134934
Desc
Variant	0031
Related	also

ClinVar
Risk	rs121913115(G;G)
Alt	rs121913115(G;G)
Reference	Rs121913115(A;A)
Significance	Pathogenic
Disease	Hypochondroplasia Short stature
Variation	info
Gene	FGFR3
CLNDBN	Hypochondroplasia Short stature
Reversed	0
HGVS	NC_000004.11:g.1803655A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017768.28, RCV000415056.1,