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rs747681609

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747681609(C;T)
Make rs747681609(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome18
Position60371856
GeneMC4R
is asnp
is mentioned by
dbSNPrs747681609
dbSNP (classic)rs747681609
ClinGenrs747681609
ebirs747681609
HLIrs747681609
Exacrs747681609
Gnomadrs747681609
Varsomers747681609
LitVarrs747681609
Maprs747681609
PheGenIrs747681609
Biobankrs747681609
1000 genomesrs747681609
hgdprs747681609
ensemblrs747681609
geneviewrs747681609
scholarrs747681609
googlers747681609
pharmgkbrs747681609
gwascentralrs747681609
openSNPrs747681609
23andMers747681609
SNPshotrs747681609
SNPdbers747681609
MSV3drs747681609
GWAS Ctlgrs747681609
Max Magnitude0
ClinVar
Risk rs747681609(T;T)
Alt rs747681609(T;T)
Reference Rs747681609(C;C)
Significance Probable-Pathogenic
Disease Obesity
Variation info
Gene MC4R
CLNDBN Obesity
Reversed 0
HGVS NC_000018.9:g.58039089C>T
CLNSRC Illumina
CLNACC RCV000332082.1,