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rs772213710

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs772213710(C;T)
Make rs772213710(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position60372069
GeneMC4R
is asnp
is mentioned by
dbSNPrs772213710
dbSNP (classic)rs772213710
ClinGenrs772213710
ebirs772213710
HLIrs772213710
Exacrs772213710
Gnomadrs772213710
Varsomers772213710
LitVarrs772213710
Maprs772213710
PheGenIrs772213710
Biobankrs772213710
1000 genomesrs772213710
hgdprs772213710
ensemblrs772213710
geneviewrs772213710
scholarrs772213710
googlers772213710
pharmgkbrs772213710
gwascentralrs772213710
openSNPrs772213710
23andMers772213710
SNPshotrs772213710
SNPdbers772213710
MSV3drs772213710
GWAS Ctlgrs772213710
Max Magnitude0
ClinVar
Risk rs772213710(T;T)
Alt rs772213710(T;T)
Reference Rs772213710(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MC4R
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.58039302C>T
CLNSRC
CLNACC RCV000432683.1,