rs121964888

Orientation

minus

Stabilized

minus

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

Make rs121964888(C;C)

Make rs121964888(C;G)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3083139

Gene

AVP

is a	snp
is	mentioned by
dbSNP	rs121964888
dbSNP (classic)	rs121964888
ClinGen	rs121964888
ebi	rs121964888
HLI	rs121964888
Exac	rs121964888
Gnomad	rs121964888
Varsome	rs121964888
LitVar	rs121964888
Map	rs121964888
PheGenI	rs121964888
Biobank	rs121964888
1000 genomes	rs121964888
hgdp	rs121964888
ensembl	rs121964888
geneview	rs121964888
scholar	rs121964888
google	rs121964888
pharmgkb	rs121964888
gwascentral	rs121964888
openSNP	rs121964888
23andMe	rs121964888
SNPshot	rs121964888
SNPdbe	rs121964888
MSV3d	rs121964888
GWAS Ctlg	rs121964888

Max Magnitude

0

OMIM	192340
Desc
Variant	0011
Related	also

ClinVar
Risk	rs121964888(C;C)
Alt	rs121964888(C;C)
Reference	Rs121964888(G;G)
Significance	Pathogenic
Disease	Neurohypophyseal diabetes insipidus
Variation	info
Gene	AVP
CLNDBN	Neurohypophyseal diabetes insipidus
Reversed	1
HGVS	NC_000020.10:g.3063785C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000012998.16,