rs121913107

Merged into

rs77722678

Orientation

minus

Stabilized

plus

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

Make rs121913107(A;C)

Make rs121913107(C;C)

Reference

GRCh38 38.1/142

Chromosome

4

Position

1805643

Gene

FGFR3

is a	snp
is	mentioned by
dbSNP	rs121913107
dbSNP (classic)	rs121913107
ClinGen	rs121913107
ebi	rs121913107
HLI	rs121913107
Exac	rs121913107
Gnomad	rs121913107
Varsome	rs121913107
LitVar	rs121913107
Map	rs121913107
PheGenI	rs121913107
Biobank	rs121913107
1000 genomes	rs121913107
hgdp	rs121913107
ensembl	rs121913107
geneview	rs121913107
scholar	rs121913107
google	rs121913107
pharmgkb	rs121913107
gwascentral	rs121913107
openSNP	rs121913107
23andMe	rs121913107
SNPshot	rs121913107
SNPdbe	rs121913107
MSV3d	rs121913107
GWAS Ctlg	rs121913107

Status

Merged into rs77722678

Max Magnitude

0

OMIM	134934
Desc
Variant	0018
Related	also

ClinVar
Risk	rs121913107(C;C)
Alt	rs121913107(C;C)
Reference	Rs121913107(A;A)
Significance	Pathogenic
Disease	Hypochondroplasia
Variation	info
Gene	FGFR3
CLNDBN	Hypochondroplasia
Reversed	0
HGVS	NC_000004.11:g.1807370A>C
CLNSRC	OMIM Allelic Variant
CLNACC	SCV000038031.1,