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rs878854420

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854420(C;C)
Make rs878854420(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position79077904
GenePHIP
is asnp
is mentioned by
dbSNPrs878854420
ebirs878854420
HLIrs878854420
Exacrs878854420
Varsomers878854420
Maprs878854420
PheGenIrs878854420
hapmaprs878854420
1000 genomesrs878854420
hgdprs878854420
ensemblrs878854420
gopubmedrs878854420
geneviewrs878854420
scholarrs878854420
googlers878854420
pharmgkbrs878854420
gwascentralrs878854420
openSNPrs878854420
23andMers878854420
23andMe allrs878854420
SNP Nexus

SNPshotrs878854420
SNPdbers878854420
MSV3drs878854420
GWAS Ctlgrs878854420
Max Magnitude0
ClinVar
Risk rs878854420(C;C)
Alt rs878854420(C;C)
Reference rs878854420(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHIP
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.79787621A>G
CLNSRC
CLNACC RCV000228040.1,