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rs199473690

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199473690(A;G)
Make rs199473690(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position10155017
GeneDNMT1
is asnp
is mentioned by
dbSNPrs199473690
ebirs199473690
HLIrs199473690
Exacrs199473690
Varsomers199473690
Maprs199473690
PheGenIrs199473690
hapmaprs199473690
1000 genomesrs199473690
hgdprs199473690
ensemblrs199473690
gopubmedrs199473690
geneviewrs199473690
scholarrs199473690
googlers199473690
pharmgkbrs199473690
gwascentralrs199473690
openSNPrs199473690
23andMers199473690
23andMe allrs199473690
SNP Nexus

SNPshotrs199473690
SNPdbers199473690
MSV3drs199473690
GWAS Ctlgrs199473690
Max Magnitude0
ClinVar
Risk rs199473690(G;G)
Alt rs199473690(G;G)
Reference rs199473690(A;A)
Significance Other
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.10265693T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000022529.28, RCV000236669.1,