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rs796052595

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052595(A;A)
Make rs796052595(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position46039701
GeneKANSL1
is asnp
is mentioned by
dbSNPrs796052595
ebirs796052595
HLIrs796052595
Exacrs796052595
Varsomers796052595
Maprs796052595
PheGenIrs796052595
hapmaprs796052595
1000 genomesrs796052595
hgdprs796052595
ensemblrs796052595
gopubmedrs796052595
geneviewrs796052595
scholarrs796052595
googlers796052595
pharmgkbrs796052595
gwascentralrs796052595
openSNPrs796052595
23andMers796052595
23andMe allrs796052595
SNP Nexus

SNPshotrs796052595
SNPdbers796052595
MSV3drs796052595
GWAS Ctlgrs796052595
Max Magnitude0
ClinVar
Risk rs796052595(A;A)
Alt rs796052595(A;A)
Reference rs796052595(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KANSL1
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.44117067C>T
CLNSRC
CLNACC RCV000187783.2,