rs2236316

Orientation

plus

Stabilized

plus

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

Make rs2236316(C;C)

Make rs2236316(C;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

50757699

Gene

NIN

is a	snp
is	mentioned by
dbSNP	rs2236316
dbSNP (classic)	rs2236316
ClinGen	rs2236316
ebi	rs2236316
HLI	rs2236316
Exac	rs2236316
Gnomad	rs2236316
Varsome	rs2236316
LitVar	rs2236316
Map	rs2236316
PheGenI	rs2236316
Biobank	rs2236316
1000 genomes	rs2236316
hgdp	rs2236316
ensembl	rs2236316
geneview	rs2236316
scholar	rs2236316
google	rs2236316
pharmgkb	rs2236316
gwascentral	rs2236316
openSNP	rs2236316
23andMe	rs2236316
SNPshot	rs2236316
SNPdbe	rs2236316
MSV3d	rs2236316
GWAS Ctlg	rs2236316

GMAF

0.1841

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

ClinVar
Risk	rs2236316(C;C)
Alt	rs2236316(C;C)
Reference	Rs2236316(G;G)
Significance	Probable-non-pathogenic
Disease	not specified
Variation	info
Gene	NIN
CLNDBN	not specified
Reversed	0
HGVS	NC_000014.8:g.51224417G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000117803.2,