rs104893649

Orientation

minus

Stabilized

minus

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

Make rs104893649(G;T)

Make rs104893649(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

181678529

Gene

NEUROD1

is a	snp
is	mentioned by
dbSNP	rs104893649
dbSNP (classic)	rs104893649
ClinGen	rs104893649
ebi	rs104893649
HLI	rs104893649
Exac	rs104893649
Gnomad	rs104893649
Varsome	rs104893649
LitVar	rs104893649
Map	rs104893649
PheGenI	rs104893649
Biobank	rs104893649
1000 genomes	rs104893649
hgdp	rs104893649
ensembl	rs104893649
geneview	rs104893649
scholar	rs104893649
google	rs104893649
pharmgkb	rs104893649
gwascentral	rs104893649
openSNP	rs104893649
23andMe	rs104893649
SNPshot	rs104893649
SNPdbe	rs104893649
MSV3d	rs104893649
GWAS Ctlg	rs104893649

Max Magnitude

0

OMIM	601724
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893649(T;T)
Alt	rs104893649(T;T)
Reference	Rs104893649(G;G)
Significance	Pathogenic
Disease	Diabetes mellitus type 2
Variation	info
Gene	NEUROD1
CLNDBN	Diabetes mellitus type 2
Reversed	1
HGVS	NC_000002.11:g.182543256C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008303.4,