rs104894611

Orientation

plus

Stabilized

plus

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

Make rs104894611(C;G)

Make rs104894611(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

56594327

Gene

NOG

is a	snp
is	mentioned by
dbSNP	rs104894611
dbSNP (classic)	rs104894611
ClinGen	rs104894611
ebi	rs104894611
HLI	rs104894611
Exac	rs104894611
Gnomad	rs104894611
Varsome	rs104894611
LitVar	rs104894611
Map	rs104894611
PheGenI	rs104894611
Biobank	rs104894611
1000 genomes	rs104894611
hgdp	rs104894611
ensembl	rs104894611
geneview	rs104894611
scholar	rs104894611
google	rs104894611
pharmgkb	rs104894611
gwascentral	rs104894611
openSNP	rs104894611
23andMe	rs104894611
SNPshot	rs104894611
SNPdbe	rs104894611
MSV3d	rs104894611
GWAS Ctlg	rs104894611

Max Magnitude

0

OMIM	602991
Desc
Variant	0007
Related	also

ClinVar
Risk	rs104894611(G;G) rs104894611(T;T)
Alt	rs104894611(G;G) rs104894611(T;T)
Reference	Rs104894611(C;C)
Significance	Pathogenic
Disease	Tarsal carpal coalition syndrome Cushing's symphalangism
Variation	info
Gene	NOG
CLNDBN	Tarsal carpal coalition syndrome Cushing's symphalangism
Reversed	0
HGVS	NC_000017.10:g.54671688C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000007085.3, RCV000049267.2,