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rs878854421

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs878854421(-;-)
Make rs878854421(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position79025986
GenePHIP
is asnp
is mentioned by
dbSNPrs878854421
ebirs878854421
HLIrs878854421
Exacrs878854421
Varsomers878854421
Maprs878854421
PheGenIrs878854421
hapmaprs878854421
1000 genomesrs878854421
hgdprs878854421
ensemblrs878854421
gopubmedrs878854421
geneviewrs878854421
scholarrs878854421
googlers878854421
pharmgkbrs878854421
gwascentralrs878854421
openSNPrs878854421
23andMers878854421
23andMe allrs878854421
SNP Nexus

SNPshotrs878854421
SNPdbers878854421
MSV3drs878854421
GWAS Ctlgrs878854421
Max Magnitude0
ClinVar
Risk rs878854421(;)
Alt rs878854421(;)
Reference rs878854421(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHIP
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.79735703delA
CLNSRC
CLNACC RCV000232097.1,