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rs796052212

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052212(A;A)
Make rs796052212(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position202334984
GeneUBE2T
is asnp
is mentioned by
dbSNPrs796052212
ebirs796052212
HLIrs796052212
Exacrs796052212
Varsomers796052212
Maprs796052212
PheGenIrs796052212
hapmaprs796052212
1000 genomesrs796052212
hgdprs796052212
ensemblrs796052212
gopubmedrs796052212
geneviewrs796052212
scholarrs796052212
googlers796052212
pharmgkbrs796052212
gwascentralrs796052212
openSNPrs796052212
23andMers796052212
23andMe allrs796052212
SNP Nexus

SNPshotrs796052212
SNPdbers796052212
MSV3drs796052212
GWAS Ctlgrs796052212
Max Magnitude0
ClinVar
Risk rs796052212(A;A)
Alt rs796052212(A;A)
Reference rs796052212(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene UBE2T
CLNDBN Fanconi anemia, complementation group t
Reversed 1
HGVS NC_000001.10:g.202304112C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000180790.3,