rs74315383

Orientation

minus

Stabilized

minus

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

Make rs74315383(G;G)

Make rs74315383(G;T)

Reference

GRCh38 38.1/141

Chromosome

20

Position

3082779

Gene

AVP

is a	snp
is	mentioned by
dbSNP	rs74315383
dbSNP (classic)	rs74315383
ClinGen	rs74315383
ebi	rs74315383
HLI	rs74315383
Exac	rs74315383
Gnomad	rs74315383
Varsome	rs74315383
LitVar	rs74315383
Map	rs74315383
PheGenI	rs74315383
Biobank	rs74315383
1000 genomes	rs74315383
hgdp	rs74315383
ensembl	rs74315383
geneview	rs74315383
scholar	rs74315383
google	rs74315383
pharmgkb	rs74315383
gwascentral	rs74315383
openSNP	rs74315383
23andMe	rs74315383
SNPshot	rs74315383
SNPdbe	rs74315383
MSV3d	rs74315383
GWAS Ctlg	rs74315383

Max Magnitude

0

OMIM	192340
Desc
Variant	0017
Related	also

ClinVar
Risk	rs74315383(G;G)
Alt	rs74315383(G;G)
Reference	Rs74315383(T;T)
Significance	Pathogenic
Disease	Neurohypophyseal diabetes insipidus
Variation	info
Gene	AVP
CLNDBN	Neurohypophyseal diabetes insipidus
Reversed	1
HGVS	NC_000020.10:g.3063425A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013004.16,