rs121964882

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs121964882(A;A)

Make rs121964882(A;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3083037

Gene

AVP

is a	snp
is	mentioned by
dbSNP	rs121964882
dbSNP (classic)	rs121964882
ClinGen	rs121964882
ebi	rs121964882
HLI	rs121964882
Exac	rs121964882
Gnomad	rs121964882
Varsome	rs121964882
LitVar	rs121964882
Map	rs121964882
PheGenI	rs121964882
Biobank	rs121964882
1000 genomes	rs121964882
hgdp	rs121964882
ensembl	rs121964882
geneview	rs121964882
scholar	rs121964882
google	rs121964882
pharmgkb	rs121964882
gwascentral	rs121964882
openSNP	rs121964882
23andMe	rs121964882
SNPshot	rs121964882
SNPdbe	rs121964882
MSV3d	rs121964882
GWAS Ctlg	rs121964882

Max Magnitude

0

OMIM	192340
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121964882(A;A)
Alt	rs121964882(A;A)
Reference	Rs121964882(G;G)
Significance	Pathogenic
Disease	Neurohypophyseal diabetes insipidus
Variation	info
Gene	AVP
CLNDBN	Neurohypophyseal diabetes insipidus
Reversed	1
HGVS	NC_000020.10:g.3063683C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012988.24,