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rs57758506

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs57758506(A;T)
Make rs57758506(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position52949556
GeneKRT8, KRT18
is asnp
is mentioned by
dbSNPrs57758506
ebirs57758506
HLIrs57758506
Exacrs57758506
Varsomers57758506
Maprs57758506
PheGenIrs57758506
hapmaprs57758506
1000 genomesrs57758506
hgdprs57758506
ensemblrs57758506
gopubmedrs57758506
geneviewrs57758506
scholarrs57758506
googlers57758506
pharmgkbrs57758506
gwascentralrs57758506
openSNPrs57758506
23andMers57758506
23andMe allrs57758506
SNP Nexus

SNPshotrs57758506
SNPdbers57758506
MSV3drs57758506
GWAS Ctlgrs57758506
Max Magnitude0
OMIM148070
Desc
Variant0001
Relatedalso
ClinVar
Risk rs57758506(T;T)
Alt rs57758506(T;T)
Reference rs57758506(A;A)
Significance Other
Disease Cirrhosis not provided
Variation info
Gene KRT8 KRT18
CLNDBN Cirrhosis, cryptogenic Cirrhosis, noncryptogenic, susceptibility to not provided
Reversed 0
HGVS NC_000012.11:g.53343340A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015686.21, RCV000015687.2, RCV000056435.1,