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rs774897991

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774897991(C;T)
Make rs774897991(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66850413
GenePC
is asnp
is mentioned by
dbSNPrs774897991
ebirs774897991
HLIrs774897991
Exacrs774897991
Varsomers774897991
Maprs774897991
PheGenIrs774897991
hapmaprs774897991
1000 genomesrs774897991
hgdprs774897991
ensemblrs774897991
gopubmedrs774897991
geneviewrs774897991
scholarrs774897991
googlers774897991
pharmgkbrs774897991
gwascentralrs774897991
openSNPrs774897991
23andMers774897991
23andMe allrs774897991
SNP Nexus

SNPshotrs774897991
SNPdbers774897991
MSV3drs774897991
GWAS Ctlgrs774897991
Max Magnitude0
ClinVar
Risk rs774897991(T;T)
Alt rs774897991(T;T)
Reference rs774897991(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.66617884C>T
CLNSRC
CLNACC RCV000186120.1,