rs121909638

Orientation

minus

Stabilized

minus

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

Make rs121909638(C;C)

Make rs121909638(C;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

38421853

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs121909638
dbSNP (classic)	rs121909638
ClinGen	rs121909638
ebi	rs121909638
HLI	rs121909638
Exac	rs121909638
Gnomad	rs121909638
Varsome	rs121909638
LitVar	rs121909638
Map	rs121909638
PheGenI	rs121909638
Biobank	rs121909638
1000 genomes	rs121909638
hgdp	rs121909638
ensembl	rs121909638
geneview	rs121909638
scholar	rs121909638
google	rs121909638
pharmgkb	rs121909638
gwascentral	rs121909638
openSNP	rs121909638
23andMe	rs121909638
SNPshot	rs121909638
SNPdbe	rs121909638
MSV3d	rs121909638
GWAS Ctlg	rs121909638

Max Magnitude

0

OMIM	136350
Desc
Variant	0017
Related	also

ClinVar
Risk	rs121909638(C;C)
Alt	rs121909638(C;C)
Reference	Rs121909638(T;T)
Significance	Other
Disease	HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA
Variation	info
Gene	FGFR1
CLNDBN	HYPOGONADOTROPIC HYPOGONADISM 2 WITH ANOSMIA, SUSCEPTIBILITY TO
Reversed	1
HGVS	NC_000008.10:g.38279371A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000030933.2,