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rs774457925

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs774457925(C;C)
Make rs774457925(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position100157309
GenePCCA
is asnp
is mentioned by
dbSNPrs774457925
ebirs774457925
HLIrs774457925
Exacrs774457925
Varsomers774457925
Maprs774457925
PheGenIrs774457925
hapmaprs774457925
1000 genomesrs774457925
hgdprs774457925
ensemblrs774457925
gopubmedrs774457925
geneviewrs774457925
scholarrs774457925
googlers774457925
pharmgkbrs774457925
gwascentralrs774457925
openSNPrs774457925
23andMers774457925
23andMe allrs774457925
SNP Nexus

SNPshotrs774457925
SNPdbers774457925
MSV3drs774457925
GWAS Ctlgrs774457925
Max Magnitude0
ClinVar
Risk rs774457925(C;C)
Alt rs774457925(C;C)
Reference rs774457925(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCA
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.100809563T>C
CLNSRC
CLNACC RCV000186079.2,