rs796065035

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(D;D)	0	common genotype

Make rs796065035(-;GG)

Make rs796065035(GG;GG)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

25161480

Gene

POMC

is a	snp
is	mentioned by
dbSNP	rs796065035
dbSNP (classic)	rs796065035
ClinGen	rs796065035
ebi	rs796065035
HLI	rs796065035
Exac	rs796065035
Gnomad	rs796065035
Varsome	rs796065035
LitVar	rs796065035
Map	rs796065035
PheGenI	rs796065035
Biobank	rs796065035
1000 genomes	rs796065035
hgdp	rs796065035
ensembl	rs796065035
geneview	rs796065035
scholar	rs796065035
google	rs796065035
pharmgkb	rs796065035
gwascentral	rs796065035
openSNP	rs796065035
23andMe	rs796065035
SNPshot	rs796065035
SNPdbe	rs796065035
MSV3d	rs796065035
GWAS Ctlg	rs796065035

Max Magnitude

0

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	RCV000014285.24,