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rs796052702

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052702(C;T)
Make rs796052702(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position39462269
GeneLIAS
is asnp
is mentioned by
dbSNPrs796052702
ebirs796052702
HLIrs796052702
Exacrs796052702
Varsomers796052702
Maprs796052702
PheGenIrs796052702
hapmaprs796052702
1000 genomesrs796052702
hgdprs796052702
ensemblrs796052702
gopubmedrs796052702
geneviewrs796052702
scholarrs796052702
googlers796052702
pharmgkbrs796052702
gwascentralrs796052702
openSNPrs796052702
23andMers796052702
23andMe allrs796052702
SNP Nexus

SNPshotrs796052702
SNPdbers796052702
MSV3drs796052702
GWAS Ctlgrs796052702
Max Magnitude0
ClinVar
Risk rs796052702(T;T)
Alt rs796052702(T;T)
Reference rs796052702(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LIAS
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.39463889C>T
CLNSRC
CLNACC RCV000188054.1,