rs77625743

Orientation

minus

Stabilized

minus

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

Make rs77625743(A;A)

Make rs77625743(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

29673368

Gene

ZFP57

is a	snp
is	mentioned by
dbSNP	rs77625743
dbSNP (classic)	rs77625743
ClinGen	rs77625743
ebi	rs77625743
HLI	rs77625743
Exac	rs77625743
Gnomad	rs77625743
Varsome	rs77625743
LitVar	rs77625743
Map	rs77625743
PheGenI	rs77625743
Biobank	rs77625743
1000 genomes	rs77625743
hgdp	rs77625743
ensembl	rs77625743
geneview	rs77625743
scholar	rs77625743
google	rs77625743
pharmgkb	rs77625743
gwascentral	rs77625743
openSNP	rs77625743
23andMe	rs77625743
SNPshot	rs77625743
SNPdbe	rs77625743
MSV3d	rs77625743
GWAS Ctlg	rs77625743

Merged from

Rs118204433

Max Magnitude

0

OMIM	612192
Desc
Variant	0005
Related	also

ClinVar
Risk	rs77625743(A;A)
Alt	rs77625743(A;A)
Reference	Rs77625743(G;G)
Significance	Pathogenic
Disease	Transient neonatal diabetes mellitus 1
Variation	info
Gene	ZFP57
CLNDBN	Transient neonatal diabetes mellitus 1
Reversed	1
HGVS	NC_000006.11:g.29641145C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000755.3,

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