rs199473692

Orientation

minus

Stabilized

minus

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

Make rs199473692(C;C)

Make rs199473692(C;T)

Reference

GRCh38 38.1/141

Chromosome

19

Position

10155018

Gene

DNMT1

is a	snp
is	mentioned by
dbSNP	rs199473692
dbSNP (classic)	rs199473692
ClinGen	rs199473692
ebi	rs199473692
HLI	rs199473692
Exac	rs199473692
Gnomad	rs199473692
Varsome	rs199473692
LitVar	rs199473692
Map	rs199473692
PheGenI	rs199473692
Biobank	rs199473692
1000 genomes	rs199473692
hgdp	rs199473692
ensembl	rs199473692
geneview	rs199473692
scholar	rs199473692
google	rs199473692
pharmgkb	rs199473692
gwascentral	rs199473692
openSNP	rs199473692
23andMe	rs199473692
SNPshot	rs199473692
SNPdbe	rs199473692
MSV3d	rs199473692
GWAS Ctlg	rs199473692

Max Magnitude

0

ClinVar
Risk	rs199473692(C;C)
Alt	rs199473692(C;C)
Reference	Rs199473692(T;T)
Significance	Pathogenic
Disease	Hereditary sensory neuropathy type IE not provided
Variation	info
Gene	DNMT1
CLNDBN	Hereditary sensory neuropathy type IE not provided
Reversed	1
HGVS	NC_000019.9:g.10265694A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000149568.3, RCV000236556.1,