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rs796065035

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796065035(-;-)
Make rs796065035(-;GG)
Make rs796065035(GG;GG)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position25161480
GenePOMC
is asnp
is mentioned by
dbSNPrs796065035
ebirs796065035
HLIrs796065035
Exacrs796065035
Varsomers796065035
Maprs796065035
PheGenIrs796065035
hapmaprs796065035
1000 genomesrs796065035
hgdprs796065035
ensemblrs796065035
gopubmedrs796065035
geneviewrs796065035
scholarrs796065035
googlers796065035
pharmgkbrs796065035
gwascentralrs796065035
openSNPrs796065035
23andMers796065035
23andMe allrs796065035
SNP Nexus

SNPshotrs796065035
SNPdbers796065035
MSV3drs796065035
GWAS Ctlgrs796065035
Max Magnitude0
ClinVar
Risk rs796065035(GG;GG)
Alt rs796065035(GG;GG)
Reference rs796065035(;)
Significance Pathogenic
Disease Proopiomelanocortin deficiency
Variation info
Gene POMC
CLNDBN Proopiomelanocortin deficiency
Reversed 1
HGVS NC_000002.11:g.25384350_25384351dupCC
CLNSRC OMIM Allelic Variant
CLNACC RCV000014285.23,