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

rs863224042

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224042(A;G)
Make rs863224042(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position197497170
GeneHSPD1
is asnp
is mentioned by
dbSNPrs863224042
ebirs863224042
HLIrs863224042
Exacrs863224042
Varsomers863224042
Maprs863224042
PheGenIrs863224042
hapmaprs863224042
1000 genomesrs863224042
hgdprs863224042
ensemblrs863224042
gopubmedrs863224042
geneviewrs863224042
scholarrs863224042
googlers863224042
pharmgkbrs863224042
gwascentralrs863224042
openSNPrs863224042
23andMers863224042
23andMe allrs863224042
SNP Nexus

SNPshotrs863224042
SNPdbers863224042
MSV3drs863224042
GWAS Ctlgrs863224042
Max Magnitude0
ClinVar
Risk rs863224042(G;G)
Alt rs863224042(G;G)
Reference rs863224042(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HSPD1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.198361894T>C
CLNSRC
CLNACC RCV000197825.1,