rs397509391

Orientation

minus

Stabilized

minus

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

Make rs397509391(G;T)

Make rs397509391(T;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

10154602

Gene

DNMT1

is a	snp
is	mentioned by
dbSNP	rs397509391
dbSNP (classic)	rs397509391
ClinGen	rs397509391
ebi	rs397509391
HLI	rs397509391
Exac	rs397509391
Gnomad	rs397509391
Varsome	rs397509391
LitVar	rs397509391
Map	rs397509391
PheGenI	rs397509391
Biobank	rs397509391
1000 genomes	rs397509391
hgdp	rs397509391
ensembl	rs397509391
geneview	rs397509391
scholar	rs397509391
google	rs397509391
pharmgkb	rs397509391
gwascentral	rs397509391
openSNP	rs397509391
23andMe	rs397509391
SNPshot	rs397509391
SNPdbe	rs397509391
MSV3d	rs397509391
GWAS Ctlg	rs397509391

Max Magnitude

0

ClinVar
Risk	rs397509391(T;T)
Alt	rs397509391(T;T)
Reference	Rs397509391(G;G)
Significance	Pathogenic
Disease	Cerebellar ataxia
Variation	info
Gene	DNMT1
CLNDBN	Cerebellar ataxia, deafness, and narcolepsy, autosomal dominant
Reversed	1
HGVS	NC_000019.9:g.10265278C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043631.29,