rs587777863

Orientation

minus

Stabilized

minus

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

Make rs587777863(C;C)

Make rs587777863(C;G)

Reference

GRCh38 38.1/142

Chromosome

3

Position

71784983

Gene	LOC105377156, PROK2

is a	snp
is	mentioned by
dbSNP	rs587777863
dbSNP (classic)	rs587777863
ClinGen	rs587777863
ebi	rs587777863
HLI	rs587777863
Exac	rs587777863
Gnomad	rs587777863
Varsome	rs587777863
LitVar	rs587777863
Map	rs587777863
PheGenI	rs587777863
Biobank	rs587777863
1000 genomes	rs587777863
hgdp	rs587777863
ensembl	rs587777863
geneview	rs587777863
scholar	rs587777863
google	rs587777863
pharmgkb	rs587777863
gwascentral	rs587777863
openSNP	rs587777863
23andMe	rs587777863
SNPshot	rs587777863
SNPdbe	rs587777863
MSV3d	rs587777863
GWAS Ctlg	rs587777863

Max Magnitude

0

ClinVar
Risk	rs587777863(C;C)
Alt	rs587777863(C;C)
Reference	Rs587777863(G;G)
Significance	Pathogenic
Disease	Kallmann syndrome 4
Variation	info
Gene	PROK2
CLNDBN	Kallmann syndrome 4
Reversed	1
HGVS	NC_000003.11:g.71834134C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000144710.3,