rs515726225

Orientation

plus

Stabilized

plus

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

Make rs515726225(A;A)

Make rs515726225(A;G)

Reference

GRCh38 38.1/142

Chromosome

8

Position

38414254

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs515726225
dbSNP (classic)	rs515726225
ClinGen	rs515726225
ebi	rs515726225
HLI	rs515726225
Exac	rs515726225
Gnomad	rs515726225
Varsome	rs515726225
LitVar	rs515726225
Map	rs515726225
PheGenI	rs515726225
Biobank	rs515726225
1000 genomes	rs515726225
hgdp	rs515726225
ensembl	rs515726225
geneview	rs515726225
scholar	rs515726225
google	rs515726225
pharmgkb	rs515726225
gwascentral	rs515726225
openSNP	rs515726225
23andMe	rs515726225
SNPshot	rs515726225
SNPdbe	rs515726225
MSV3d	rs515726225
GWAS Ctlg	rs515726225

Max Magnitude

0

ClinVar
Risk	rs515726225(A;A)
Alt	rs515726225(A;A)
Reference	Rs515726225(G;G)
Significance	Pathogenic
Disease	Kallmann syndrome 2
Variation	info
Gene	FGFR1
CLNDBN	Kallmann syndrome 2
Reversed	0
HGVS	NC_000008.10:g.38271772G>A
CLNSRC	ClinVar Pin India
CLNACC	RCV000119060.1,