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rs1017182331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position97739386
GeneZAP70
is asnp
is mentioned by
dbSNPrs1017182331
dbSNP (classic)rs1017182331
ClinGenrs1017182331
ebirs1017182331
HLIrs1017182331
Exacrs1017182331
Gnomadrs1017182331
Varsomers1017182331
LitVarrs1017182331
Maprs1017182331
PheGenIrs1017182331
Biobankrs1017182331
1000 genomesrs1017182331
hgdprs1017182331
ensemblrs1017182331
geneviewrs1017182331
scholarrs1017182331
googlers1017182331
pharmgkbrs1017182331
gwascentralrs1017182331
openSNPrs1017182331
23andMers1017182331
23andMe allrs1017182331
SNPshotrs1017182331
SNPdbers1017182331
MSV3drs1017182331
GWAS Ctlgrs1017182331
Max Magnitude0
ClinVar
Risk rs1017182331(A;A)
Alt rs1017182331(A;A)
Reference Rs1017182331(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.98355849G>A
CLNSRC
CLNACC RCV000484238.1,