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rs774357609

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs774357609(C;C)
Make rs774357609(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position202335751
GeneUBE2T
is asnp
is mentioned by
dbSNPrs774357609
ebirs774357609
HLIrs774357609
Exacrs774357609
Varsomers774357609
Maprs774357609
PheGenIrs774357609
hapmaprs774357609
1000 genomesrs774357609
hgdprs774357609
ensemblrs774357609
gopubmedrs774357609
geneviewrs774357609
scholarrs774357609
googlers774357609
pharmgkbrs774357609
gwascentralrs774357609
openSNPrs774357609
23andMers774357609
23andMe allrs774357609
SNP Nexus

SNPshotrs774357609
SNPdbers774357609
MSV3drs774357609
GWAS Ctlgrs774357609
Max Magnitude0
ClinVar
Risk rs774357609(C;C)
Alt rs774357609(C;C)
Reference rs774357609(G;G)
Significance Pathogenic
Disease Fanconi anemia
Variation info
Gene UBE2T
CLNDBN Fanconi anemia, complementation group t
Reversed 0
HGVS NC_000001.10:g.202304879G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000180789.3,