rs79020217

Orientation

minus

Stabilized

minus

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

Make rs79020217(C;G)

Make rs79020217(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

29672739

Gene	MOG, ZFP57

is a	snp
is	mentioned by
dbSNP	rs79020217
dbSNP (classic)	rs79020217
ClinGen	rs79020217
ebi	rs79020217
HLI	rs79020217
Exac	rs79020217
Gnomad	rs79020217
Varsome	rs79020217
LitVar	rs79020217
Map	rs79020217
PheGenI	rs79020217
Biobank	rs79020217
1000 genomes	rs79020217
hgdp	rs79020217
ensembl	rs79020217
geneview	rs79020217
scholar	rs79020217
google	rs79020217
pharmgkb	rs79020217
gwascentral	rs79020217
openSNP	rs79020217
23andMe	rs79020217
SNPshot	rs79020217
SNPdbe	rs79020217
MSV3d	rs79020217
GWAS Ctlg	rs79020217

Merged from

Rs118204432

Max Magnitude

0

OMIM	612192
Desc
Variant	0004
Related	also

ClinVar
Risk	rs79020217(G;G)
Alt	rs79020217(G;G)
Reference	Rs79020217(C;C)
Significance	Pathogenic
Disease	Transient neonatal diabetes mellitus 1
Variation	info
Gene	MOG ZFP57
CLNDBN	Transient neonatal diabetes mellitus 1
Reversed	1
HGVS	NC_000006.11:g.29640516G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000754.3,

[PMID 18622393] Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.