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rs200030109

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200030109(A;A)
Make rs200030109(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66870419
GenePC
is asnp
is mentioned by
dbSNPrs200030109
ebirs200030109
HLIrs200030109
Exacrs200030109
Varsomers200030109
Maprs200030109
PheGenIrs200030109
hapmaprs200030109
1000 genomesrs200030109
hgdprs200030109
ensemblrs200030109
gopubmedrs200030109
geneviewrs200030109
scholarrs200030109
googlers200030109
pharmgkbrs200030109
gwascentralrs200030109
openSNPrs200030109
23andMers200030109
23andMe allrs200030109
SNP Nexus

SNPshotrs200030109
SNPdbers200030109
MSV3drs200030109
GWAS Ctlgrs200030109
Max Magnitude0
ClinVar
Risk rs200030109(A;A)
Alt rs200030109(A;A)
Reference rs200030109(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.66637890C>A
CLNSRC
CLNACC RCV000186122.1,