rs137853238

Orientation

plus

Stabilized

plus

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

Make rs137853238(A;A)

Make rs137853238(A;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

120994265

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs137853238
dbSNP (classic)	rs137853238
ClinGen	rs137853238
ebi	rs137853238
HLI	rs137853238
Exac	rs137853238
Gnomad	rs137853238
Varsome	rs137853238
LitVar	rs137853238
Map	rs137853238
PheGenI	rs137853238
Biobank	rs137853238
1000 genomes	rs137853238
hgdp	rs137853238
ensembl	rs137853238
geneview	rs137853238
scholar	rs137853238
google	rs137853238
pharmgkb	rs137853238
gwascentral	rs137853238
openSNP	rs137853238
23andMe	rs137853238
SNPshot	rs137853238
SNPdbe	rs137853238
MSV3d	rs137853238
GWAS Ctlg	rs137853238

Max Magnitude

0

OMIM	142410
Desc
Variant	0005
Related	also

ClinVar
Risk	rs137853238(A;A)
Alt	rs137853238(A;A)
Reference	Rs137853238(G;G)
Significance	Pathogenic
Disease	Diabetes mellitus not provided Monogenic diabetes
Variation	info
Gene	HNF1A
CLNDBN	Diabetes mellitus, insulin-dependent, 20 not provided Monogenic diabetes
Reversed	0
HGVS	NC_000012.11:g.121432068G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016068.23, RCV000255916.1, RCV000445525.1,