rs1060499663

Orientation

minus

Stabilized

minus

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

Make rs1060499663(-;-)

Make rs1060499663(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

38416013

Gene

FGFR1

is a	snp
is	mentioned by
dbSNP	rs1060499663
dbSNP (classic)	rs1060499663
ClinGen	rs1060499663
ebi	rs1060499663
HLI	rs1060499663
Exac	rs1060499663
Gnomad	rs1060499663
Varsome	rs1060499663
LitVar	rs1060499663
Map	rs1060499663
PheGenI	rs1060499663
Biobank	rs1060499663
1000 genomes	rs1060499663
hgdp	rs1060499663
ensembl	rs1060499663
geneview	rs1060499663
scholar	rs1060499663
google	rs1060499663
pharmgkb	rs1060499663
gwascentral	rs1060499663
openSNP	rs1060499663
23andMe	rs1060499663
SNPshot	rs1060499663
SNPdbe	rs1060499663
MSV3d	rs1060499663
GWAS Ctlg	rs1060499663

Max Magnitude

0

ClinVar
Risk	rs1060499663(-;-)
Alt	rs1060499663(-;-)
Reference	Rs1060499663(G;G)
Significance	Pathogenic
Disease	Kallmann syndrome 2
Variation	info
Gene	FGFR1
CLNDBN	Kallmann syndrome 2
Reversed	1
HGVS	NC_000008.10:g.38273531delC
CLNSRC
CLNACC	RCV000449624.1,