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rs770045008

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs770045008(C;T)
Make rs770045008(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position35503626
GeneTULP1
is asnp
is mentioned by
dbSNPrs770045008
ebirs770045008
HLIrs770045008
Exacrs770045008
Varsomers770045008
Maprs770045008
PheGenIrs770045008
hapmaprs770045008
1000 genomesrs770045008
hgdprs770045008
ensemblrs770045008
gopubmedrs770045008
geneviewrs770045008
scholarrs770045008
googlers770045008
pharmgkbrs770045008
gwascentralrs770045008
openSNPrs770045008
23andMers770045008
23andMe allrs770045008
SNP Nexus

SNPshotrs770045008
SNPdbers770045008
MSV3drs770045008
GWAS Ctlgrs770045008
Max Magnitude0
ClinVar
Risk rs770045008(T;T)
Alt rs770045008(T;T)
Reference rs770045008(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TULP1
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.35471403C>T
CLNSRC
CLNACC RCV000171394.1,