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rs767745816

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs767745816(A;A)
Make rs767745816(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position88416760
GeneSPATA7
is asnp
is mentioned by
dbSNPrs767745816
ebirs767745816
HLIrs767745816
Exacrs767745816
Varsomers767745816
Maprs767745816
PheGenIrs767745816
hapmaprs767745816
1000 genomesrs767745816
hgdprs767745816
ensemblrs767745816
gopubmedrs767745816
geneviewrs767745816
scholarrs767745816
googlers767745816
pharmgkbrs767745816
gwascentralrs767745816
openSNPrs767745816
23andMers767745816
23andMe allrs767745816
SNP Nexus

SNPshotrs767745816
SNPdbers767745816
MSV3drs767745816
GWAS Ctlgrs767745816
Max Magnitude0
ClinVar
Risk rs767745816(A;A)
Alt rs767745816(A;A)
Reference rs767745816(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPATA7
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.88883104T>A
CLNSRC
CLNACC RCV000171226.1,