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rs757982865

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs757982865(G;G)
Make rs757982865(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position140647330
GeneIK, MIR3655, NDUFA2, TMCO6
is asnp
is mentioned by
dbSNPrs757982865
ebirs757982865
HLIrs757982865
Exacrs757982865
Varsomers757982865
Maprs757982865
PheGenIrs757982865
hapmaprs757982865
1000 genomesrs757982865
hgdprs757982865
ensemblrs757982865
gopubmedrs757982865
geneviewrs757982865
scholarrs757982865
googlers757982865
pharmgkbrs757982865
gwascentralrs757982865
openSNPrs757982865
23andMers757982865
23andMe allrs757982865
SNP Nexus

SNPshotrs757982865
SNPdbers757982865
MSV3drs757982865
GWAS Ctlgrs757982865
Max Magnitude0
ClinVar
Risk rs757982865(G;G)
Alt rs757982865(G;G)
Reference rs757982865(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR3655 NDUFA2 IK
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.140026915T>G
CLNSRC
CLNACC RCV000200612.1,