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rs201727685

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201727685(C;C)
Make rs201727685(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position67608562
GeneC11orf72, NDUFV1
is asnp
is mentioned by
dbSNPrs201727685
dbSNP (classic)rs201727685
ClinGenrs201727685
ebirs201727685
HLIrs201727685
Exacrs201727685
Gnomadrs201727685
Varsomers201727685
LitVarrs201727685
Maprs201727685
PheGenIrs201727685
Biobankrs201727685
1000 genomesrs201727685
hgdprs201727685
ensemblrs201727685
geneviewrs201727685
scholarrs201727685
googlers201727685
pharmgkbrs201727685
gwascentralrs201727685
openSNPrs201727685
23andMers201727685
SNPshotrs201727685
SNPdbers201727685
MSV3drs201727685
GWAS Ctlgrs201727685
Max Magnitude0
ClinVar
Risk rs201727685(C;C)
Alt rs201727685(C;C)
Reference Rs201727685(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFV1 C11orf72
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67376033T>C
CLNSRC
CLNACC RCV000413903.1,