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rs797044953

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044953(A;T)
Make rs797044953(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position9447684
GeneSETD5
is asnp
is mentioned by
dbSNPrs797044953
ebirs797044953
HLIrs797044953
Exacrs797044953
Varsomers797044953
Maprs797044953
PheGenIrs797044953
hapmaprs797044953
1000 genomesrs797044953
hgdprs797044953
ensemblrs797044953
gopubmedrs797044953
geneviewrs797044953
scholarrs797044953
googlers797044953
pharmgkbrs797044953
gwascentralrs797044953
openSNPrs797044953
23andMers797044953
23andMe allrs797044953
SNP Nexus

SNPshotrs797044953
SNPdbers797044953
MSV3drs797044953
GWAS Ctlgrs797044953
Max Magnitude0
ClinVar
Risk rs797044953(T;T)
Alt rs797044953(T;T)
Reference rs797044953(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SETD5
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000003.11:g.9489368A>T
CLNSRC
CLNACC RCV000190808.1,