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rs771013055

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771013055(G;T)
Make rs771013055(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position65719800
GeneKAT5, RNASEH2C
is asnp
is mentioned by
dbSNPrs771013055
ebirs771013055
HLIrs771013055
Exacrs771013055
Varsomers771013055
Maprs771013055
PheGenIrs771013055
hapmaprs771013055
1000 genomesrs771013055
hgdprs771013055
ensemblrs771013055
gopubmedrs771013055
geneviewrs771013055
scholarrs771013055
googlers771013055
pharmgkbrs771013055
gwascentralrs771013055
openSNPrs771013055
23andMers771013055
23andMe allrs771013055
SNP Nexus

SNPshotrs771013055
SNPdbers771013055
MSV3drs771013055
GWAS Ctlgrs771013055
Max Magnitude0
ClinVar
Risk rs771013055(A,T;A,T)
Alt rs771013055(A,T;A,T)
Reference rs771013055(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KAT5 RNASEH2C
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.65487271G>A
CLNSRC
CLNACC RCV000171197.1,