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rs199473692

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199473692(C;C)
Make rs199473692(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position10155018
GeneDNMT1
is asnp
is mentioned by
dbSNPrs199473692
ebirs199473692
HLIrs199473692
Exacrs199473692
Varsomers199473692
Maprs199473692
PheGenIrs199473692
hapmaprs199473692
1000 genomesrs199473692
hgdprs199473692
ensemblrs199473692
gopubmedrs199473692
geneviewrs199473692
scholarrs199473692
googlers199473692
pharmgkbrs199473692
gwascentralrs199473692
openSNPrs199473692
23andMers199473692
23andMe allrs199473692
SNP Nexus

SNPshotrs199473692
SNPdbers199473692
MSV3drs199473692
GWAS Ctlgrs199473692
Max Magnitude0
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,