rs137852659

Orientation

minus

Stabilized

minus

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

Make rs137852659(A;A)

Make rs137852659(A;C)

Reference

GRCh38 38.1/141

Chromosome

10

Position

101775769

Gene

FGF8

is a	snp
is	mentioned by
dbSNP	rs137852659
dbSNP (classic)	rs137852659
ClinGen	rs137852659
ebi	rs137852659
HLI	rs137852659
Exac	rs137852659
Gnomad	rs137852659
Varsome	rs137852659
LitVar	rs137852659
Map	rs137852659
PheGenI	rs137852659
Biobank	rs137852659
1000 genomes	rs137852659
hgdp	rs137852659
ensembl	rs137852659
geneview	rs137852659
scholar	rs137852659
google	rs137852659
pharmgkb	rs137852659
gwascentral	rs137852659
openSNP	rs137852659
23andMe	rs137852659
SNPshot	rs137852659
SNPdbe	rs137852659
MSV3d	rs137852659
GWAS Ctlg	rs137852659

Max Magnitude

0

OMIM	600483
Desc
Variant	0001
Related	also

ClinVar
Risk	rs137852659(A;A)
Alt	rs137852659(A;A)
Reference	Rs137852659(C;C)
Significance	Pathogenic
Disease	Kallmann syndrome 6
Variation	info
Gene	FGF8
CLNDBN	Kallmann syndrome 6
Reversed	1
HGVS	NC_000010.10:g.103535526G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000030886.2,