rs121909629

Orientation

minus

Stabilized

minus

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

Make rs121909629(A;A)

Make rs121909629(A;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

38415905

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs121909629
dbSNP (classic)	rs121909629
ClinGen	rs121909629
ebi	rs121909629
HLI	rs121909629
Exac	rs121909629
Gnomad	rs121909629
Varsome	rs121909629
LitVar	rs121909629
Map	rs121909629
PheGenI	rs121909629
Biobank	rs121909629
1000 genomes	rs121909629
hgdp	rs121909629
ensembl	rs121909629
geneview	rs121909629
scholar	rs121909629
google	rs121909629
pharmgkb	rs121909629
gwascentral	rs121909629
openSNP	rs121909629
23andMe	rs121909629
SNPshot	rs121909629
SNPdbe	rs121909629
MSV3d	rs121909629
GWAS Ctlg	rs121909629

Max Magnitude

0

OMIM	136350
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121909629(A;A)
Alt	rs121909629(A;A)
Reference	Rs121909629(G;G)
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.38273423C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000030927.3,