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rs796051989

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796051989(A;T)
Make rs796051989(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
is asnp
is mentioned by
dbSNPrs796051989
ebirs796051989
HLIrs796051989
Exacrs796051989
Varsomers796051989
Maprs796051989
PheGenIrs796051989
hapmaprs796051989
1000 genomesrs796051989
hgdprs796051989
ensemblrs796051989
gopubmedrs796051989
geneviewrs796051989
scholarrs796051989
googlers796051989
pharmgkbrs796051989
gwascentralrs796051989
openSNPrs796051989
23andMers796051989
23andMe allrs796051989
SNP Nexus

SNPshotrs796051989
SNPdbers796051989
MSV3drs796051989
GWAS Ctlgrs796051989
Max Magnitude0
ClinVar
Risk rs796051989(T;T)
Alt rs796051989(T;T)
Reference rs796051989(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.70888813A>T
CLNSRC
CLNACC RCV000186004.1,