Have questions? Visit https://www.reddit.com/r/SNPedia

rs769177104

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769177104(C;T)
Make rs769177104(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66870417
GenePC
is asnp
is mentioned by
dbSNPrs769177104
ebirs769177104
HLIrs769177104
Exacrs769177104
Varsomers769177104
Maprs769177104
PheGenIrs769177104
hapmaprs769177104
1000 genomesrs769177104
hgdprs769177104
ensemblrs769177104
gopubmedrs769177104
geneviewrs769177104
scholarrs769177104
googlers769177104
pharmgkbrs769177104
gwascentralrs769177104
openSNPrs769177104
23andMers769177104
23andMe allrs769177104
SNP Nexus

SNPshotrs769177104
SNPdbers769177104
MSV3drs769177104
GWAS Ctlgrs769177104
Max Magnitude0
ClinVar
Risk rs769177104(T;T)
Alt rs769177104(T;T)
Reference rs769177104(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.66637888C>T
CLNSRC
CLNACC RCV000186127.1,