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rs1057517991

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517991(C;C)
Make rs1057517991(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position60371539
GeneMC4R
is asnp
is mentioned by
dbSNPrs1057517991
dbSNP (old)rs1057517991
ClinGenrs1057517991
ebirs1057517991
HLIrs1057517991
Exacrs1057517991
Gnomadrs1057517991
Varsomers1057517991
Maprs1057517991
PheGenIrs1057517991
Biobankrs1057517991
1000 genomesrs1057517991
hgdprs1057517991
ensemblrs1057517991
gopubmedrs1057517991
geneviewrs1057517991
scholarrs1057517991
googlers1057517991
pharmgkbrs1057517991
gwascentralrs1057517991
openSNPrs1057517991
23andMers1057517991
23andMe allrs1057517991
SNPshotrs1057517991
SNPdbers1057517991
MSV3drs1057517991
GWAS Ctlgrs1057517991
Max Magnitude0
ClinVar
Risk rs1057517991(C;C)
Alt rs1057517991(C;C)
Reference Rs1057517991(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene MC4R
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.58038772A>G
CLNSRC
CLNACC RCV000413435.1,