rs606231408

Orientation

minus

Stabilized

minus

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

Make rs606231408(C;G)

Make rs606231408(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

10

Position

101774832

Gene

FGF8

is a	snp
is	mentioned by
dbSNP	rs606231408
dbSNP (classic)	rs606231408
ClinGen	rs606231408
ebi	rs606231408
HLI	rs606231408
Exac	rs606231408
Gnomad	rs606231408
Varsome	rs606231408
LitVar	rs606231408
Map	rs606231408
PheGenI	rs606231408
Biobank	rs606231408
1000 genomes	rs606231408
hgdp	rs606231408
ensembl	rs606231408
geneview	rs606231408
scholar	rs606231408
google	rs606231408
pharmgkb	rs606231408
gwascentral	rs606231408
openSNP	rs606231408
23andMe	rs606231408
SNPshot	rs606231408
SNPdbe	rs606231408
MSV3d	rs606231408
GWAS Ctlg	rs606231408

Max Magnitude

0

ClinVar
Risk	rs606231408(G;G)
Alt	rs606231408(G;G)
Reference	Rs606231408(C;C)
Significance	Probable-Pathogenic
Disease	Kallmann syndrome 6
Variation	info
Gene	FGF8
CLNDBN	Kallmann syndrome 6
Reversed	1
HGVS	NC_000010.10:g.103534589G>C
CLNSRC
CLNACC	RCV000128829.1,