rs76736111

Orientation

plus

Stabilized

plus

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

Make rs76736111(A;A)

Make rs76736111(A;C)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43102596

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs76736111
dbSNP (classic)	rs76736111
ClinGen	rs76736111
ebi	rs76736111
HLI	rs76736111
Exac	rs76736111
Gnomad	rs76736111
Varsome	rs76736111
LitVar	rs76736111
Map	rs76736111
PheGenI	rs76736111
Biobank	rs76736111
1000 genomes	rs76736111
hgdp	rs76736111
ensembl	rs76736111
geneview	rs76736111
scholar	rs76736111
google	rs76736111
pharmgkb	rs76736111
gwascentral	rs76736111
openSNP	rs76736111
23andMe	rs76736111
SNPshot	rs76736111
SNPdbe	rs76736111
MSV3d	rs76736111
GWAS Ctlg	rs76736111

Max Magnitude

0

OMIM	164761
Desc
Variant	0054
Related	also

ClinVar
Risk	rs76736111(A;A)
Alt	rs76736111(A;A)
Reference	Rs76736111(C;C)
Significance	Pathogenic
Disease	Renal adysplasia
Variation	info
Gene	RET
CLNDBN	Renal adysplasia
Reversed	0
HGVS	NC_000010.10:g.43598044C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014984.22,