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rs143511416

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs143511416(C;T)
Make rs143511416(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position196217066
GeneHECW2
is asnp
is mentioned by
dbSNPrs143511416
dbSNP (old)rs143511416
ClinGenrs143511416
ebirs143511416
HLIrs143511416
Exacrs143511416
Gnomadrs143511416
Varsomers143511416
Maprs143511416
PheGenIrs143511416
Biobankrs143511416
1000 genomesrs143511416
hgdprs143511416
ensemblrs143511416
gopubmedrs143511416
geneviewrs143511416
scholarrs143511416
googlers143511416
pharmgkbrs143511416
gwascentralrs143511416
openSNPrs143511416
23andMers143511416
23andMe allrs143511416
SNPshotrs143511416
SNPdbers143511416
MSV3drs143511416
GWAS Ctlgrs143511416
Max Magnitude0
ClinVar
Risk rs143511416(T;T)
Alt rs143511416(T;T)
Reference Rs143511416(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HECW2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.197081790C>T
CLNSRC
CLNACC RCV000442124.1,