rs121964889

Orientation

minus

Stabilized

minus

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

Make rs121964889(G;T)

Make rs121964889(T;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3082788

Gene

AVP

is a	snp
is	mentioned by
dbSNP	rs121964889
dbSNP (classic)	rs121964889
ClinGen	rs121964889
ebi	rs121964889
HLI	rs121964889
Exac	rs121964889
Gnomad	rs121964889
Varsome	rs121964889
LitVar	rs121964889
Map	rs121964889
PheGenI	rs121964889
Biobank	rs121964889
1000 genomes	rs121964889
hgdp	rs121964889
ensembl	rs121964889
geneview	rs121964889
scholar	rs121964889
google	rs121964889
pharmgkb	rs121964889
gwascentral	rs121964889
openSNP	rs121964889
23andMe	rs121964889
SNPshot	rs121964889
SNPdbe	rs121964889
MSV3d	rs121964889
GWAS Ctlg	rs121964889

Max Magnitude

0

OMIM	192340
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121964889(A;A) rs121964889(T;T)
Alt	rs121964889(A;A) rs121964889(T;T)
Reference	Rs121964889(G;G)
Significance	Pathogenic
Disease	Neurohypophyseal diabetes insipidus
Variation	info
Gene	AVP
CLNDBN	Neurohypophyseal diabetes insipidus
Reversed	1
HGVS	NC_000020.10:g.3063434C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000012999.22,