rs137852664

Orientation

minus

Stabilized

minus

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

Make rs137852664(C;T)

Make rs137852664(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

101770378

Gene	FGF8, LOC105378457

is a	snp
is	mentioned by
dbSNP	rs137852664
dbSNP (classic)	rs137852664
ClinGen	rs137852664
ebi	rs137852664
HLI	rs137852664
Exac	rs137852664
Gnomad	rs137852664
Varsome	rs137852664
LitVar	rs137852664
Map	rs137852664
PheGenI	rs137852664
Biobank	rs137852664
1000 genomes	rs137852664
hgdp	rs137852664
ensembl	rs137852664
geneview	rs137852664
scholar	rs137852664
google	rs137852664
pharmgkb	rs137852664
gwascentral	rs137852664
openSNP	rs137852664
23andMe	rs137852664
SNPshot	rs137852664
SNPdbe	rs137852664
MSV3d	rs137852664
GWAS Ctlg	rs137852664

Max Magnitude

0

OMIM	600483
Desc
Variant	0006
Related	also

ClinVar
Risk	rs137852664(T;T)
Alt	rs137852664(T;T)
Reference	Rs137852664(C;C)
Significance	Unknown
Disease	Kallmann syndrome 6
Variation	info
Gene	FGF8
CLNDBN	Kallmann syndrome 6
Reversed	1
HGVS	NC_000010.10:g.103530135G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009697.2,