rs104894610

Orientation

plus

Stabilized

plus

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

Make rs104894610(G;T)

Make rs104894610(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

56594834

Gene

NOG

is a	snp
is	mentioned by
dbSNP	rs104894610
dbSNP (classic)	rs104894610
ClinGen	rs104894610
ebi	rs104894610
HLI	rs104894610
Exac	rs104894610
Gnomad	rs104894610
Varsome	rs104894610
LitVar	rs104894610
Map	rs104894610
PheGenI	rs104894610
Biobank	rs104894610
1000 genomes	rs104894610
hgdp	rs104894610
ensembl	rs104894610
geneview	rs104894610
scholar	rs104894610
google	rs104894610
pharmgkb	rs104894610
gwascentral	rs104894610
openSNP	rs104894610
23andMe	rs104894610
SNPshot	rs104894610
SNPdbe	rs104894610
MSV3d	rs104894610
GWAS Ctlg	rs104894610

Max Magnitude

0

OMIM	602991
Desc
Variant	0006
Related	also

ClinVar
Risk	rs104894610(A;A) rs104894610(T;T)
Alt	rs104894610(A;A) rs104894610(T;T)
Reference	Rs104894610(G;G)
Significance	Pathogenic
Disease	Tarsal carpal coalition syndrome
Variation	info
Gene	NOG
CLNDBN	Tarsal carpal coalition syndrome
Reversed	0
HGVS	NC_000017.10:g.54672195G>A; NC_000017.10:g.54672195G>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000416327.1, RCV000007084.2,