rs193922486

Orientation

minus

Stabilized

minus

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

Make rs193922486(A;A)

Make rs193922486(A;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

37744664

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs193922486
dbSNP (classic)	rs193922486
ClinGen	rs193922486
ebi	rs193922486
HLI	rs193922486
Exac	rs193922486
Gnomad	rs193922486
Varsome	rs193922486
LitVar	rs193922486
Map	rs193922486
PheGenI	rs193922486
Biobank	rs193922486
1000 genomes	rs193922486
hgdp	rs193922486
ensembl	rs193922486
geneview	rs193922486
scholar	rs193922486
google	rs193922486
pharmgkb	rs193922486
gwascentral	rs193922486
openSNP	rs193922486
23andMe	rs193922486
SNPshot	rs193922486
SNPdbe	rs193922486
MSV3d	rs193922486
GWAS Ctlg	rs193922486

Max Magnitude

0

ClinVar
Risk	rs193922486(A;A)
Alt	rs193922486(A;A)
Reference	Rs193922486(T;T)
Significance	Probable-Pathogenic
Disease	Familial hypoplastic
Variation	info
Gene	HNF1B
CLNDBN	Familial hypoplastic, glomerulocystic kidney
Reversed	1
HGVS	NC_000017.10:g.36104655A>T
CLNSRC	ClinVar
CLNACC	RCV000030526.1,