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rs749056160

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749056160(C;T)
Make rs749056160(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position125059395
GeneKIAA0196
is asnp
is mentioned by
dbSNPrs749056160
ebirs749056160
HLIrs749056160
Exacrs749056160
Varsomers749056160
Maprs749056160
PheGenIrs749056160
hapmaprs749056160
1000 genomesrs749056160
hgdprs749056160
ensemblrs749056160
gopubmedrs749056160
geneviewrs749056160
scholarrs749056160
googlers749056160
pharmgkbrs749056160
gwascentralrs749056160
openSNPrs749056160
23andMers749056160
23andMe allrs749056160
SNP Nexus

SNPshotrs749056160
SNPdbers749056160
MSV3drs749056160
GWAS Ctlgrs749056160
Max Magnitude0
ClinVar
Risk rs749056160(T;T)
Alt rs749056160(T;T)
Reference rs749056160(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KIAA0196
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.126071637C>T
CLNSRC
CLNACC RCV000171420.1,