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rs201956469

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201956469(C;T)
Make rs201956469(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position56621697
GeneTMEM260
is asnp
is mentioned by
dbSNPrs201956469
dbSNP (old)rs201956469
ClinGenrs201956469
ebirs201956469
HLIrs201956469
Exacrs201956469
Gnomadrs201956469
Varsomers201956469
Maprs201956469
PheGenIrs201956469
Biobankrs201956469
1000 genomesrs201956469
hgdprs201956469
ensemblrs201956469
gopubmedrs201956469
geneviewrs201956469
scholarrs201956469
googlers201956469
pharmgkbrs201956469
gwascentralrs201956469
openSNPrs201956469
23andMers201956469
23andMe allrs201956469
SNPshotrs201956469
SNPdbers201956469
MSV3drs201956469
GWAS Ctlgrs201956469
Max Magnitude0
ClinVar
Risk rs201956469(T;T)
Alt rs201956469(T;T)
Reference Rs201956469(C;C)
Significance Pathogenic
Disease Structural heart defects and renal anomalies syndrome
Variation info
Gene TMEM260
CLNDBN Structural heart defects and renal anomalies syndrome
Reversed 0
HGVS NC_000014.8:g.57088415C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000488880.1,