rs137852661

Orientation

minus

Stabilized

minus

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

Make rs137852661(C;C)

Make rs137852661(C;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

101775168

Gene

FGF8

is a	snp
is	mentioned by
dbSNP	rs137852661
dbSNP (classic)	rs137852661
ClinGen	rs137852661
ebi	rs137852661
HLI	rs137852661
Exac	rs137852661
Gnomad	rs137852661
Varsome	rs137852661
LitVar	rs137852661
Map	rs137852661
PheGenI	rs137852661
Biobank	rs137852661
1000 genomes	rs137852661
hgdp	rs137852661
ensembl	rs137852661
geneview	rs137852661
scholar	rs137852661
google	rs137852661
pharmgkb	rs137852661
gwascentral	rs137852661
openSNP	rs137852661
23andMe	rs137852661
SNPshot	rs137852661
SNPdbe	rs137852661
MSV3d	rs137852661
GWAS Ctlg	rs137852661

Max Magnitude

0

OMIM	600483
Desc
Variant	0003
Related	also

ClinVar
Risk	rs137852661(C;C)
Alt	rs137852661(C;C)
Reference	Rs137852661(T;T)
Significance	Pathogenic
Disease	Kallmann syndrome 6
Variation	info
Gene	FGF8
CLNDBN	Kallmann syndrome 6
Reversed	1
HGVS	NC_000010.10:g.103534925A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000030887.2,