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rs796052603

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052603(C;T)
Make rs796052603(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position46170958
GeneKANSL1, LOC105376838
is asnp
is mentioned by
dbSNPrs796052603
ebirs796052603
HLIrs796052603
Exacrs796052603
Varsomers796052603
Maprs796052603
PheGenIrs796052603
hapmaprs796052603
1000 genomesrs796052603
hgdprs796052603
ensemblrs796052603
gopubmedrs796052603
geneviewrs796052603
scholarrs796052603
googlers796052603
pharmgkbrs796052603
gwascentralrs796052603
openSNPrs796052603
23andMers796052603
23andMe allrs796052603
SNP Nexus

SNPshotrs796052603
SNPdbers796052603
MSV3drs796052603
GWAS Ctlgrs796052603
Max Magnitude0
ClinVar
Risk rs796052603(T;T)
Alt rs796052603(T;T)
Reference rs796052603(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KANSL1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.44248324G>A
CLNSRC
CLNACC RCV000187802.1,