rs121964886

Orientation

minus

Stabilized

minus

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

Make rs121964886(G;T)

Make rs121964886(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3083012

Gene

AVP

is a	snp
is	mentioned by
dbSNP	rs121964886
dbSNP (classic)	rs121964886
ClinGen	rs121964886
ebi	rs121964886
HLI	rs121964886
Exac	rs121964886
Gnomad	rs121964886
Varsome	rs121964886
LitVar	rs121964886
Map	rs121964886
PheGenI	rs121964886
Biobank	rs121964886
1000 genomes	rs121964886
hgdp	rs121964886
ensembl	rs121964886
geneview	rs121964886
scholar	rs121964886
google	rs121964886
pharmgkb	rs121964886
gwascentral	rs121964886
openSNP	rs121964886
23andMe	rs121964886
SNPshot	rs121964886
SNPdbe	rs121964886
MSV3d	rs121964886
GWAS Ctlg	rs121964886

Max Magnitude

0

OMIM	192340
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121964886(T;T)
Alt	rs121964886(T;T)
Reference	Rs121964886(G;G)
Significance	Pathogenic
Disease	Neurohypophyseal diabetes insipidus
Variation	info
Gene	AVP
CLNDBN	Neurohypophyseal diabetes insipidus
Reversed	1
HGVS	NC_000020.10:g.3063658C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012995.22,