rs76534745

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs76534745(A;G)

Make rs76534745(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43123783

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs76534745
dbSNP (classic)	rs76534745
ClinGen	rs76534745
ebi	rs76534745
HLI	rs76534745
Exac	rs76534745
Gnomad	rs76534745
Varsome	rs76534745
LitVar	rs76534745
Map	rs76534745
PheGenI	rs76534745
Biobank	rs76534745
1000 genomes	rs76534745
hgdp	rs76534745
ensembl	rs76534745
geneview	rs76534745
scholar	rs76534745
google	rs76534745
pharmgkb	rs76534745
gwascentral	rs76534745
openSNP	rs76534745
23andMe	rs76534745
SNPshot	rs76534745
SNPdbe	rs76534745
MSV3d	rs76534745
GWAS Ctlg	rs76534745

Max Magnitude

0

OMIM	164761
Desc
Variant	0017
Related	also

ClinVar
Risk	rs76534745(G;G)
Alt	rs76534745(G;G)
Reference	Rs76534745(A;A)
Significance	Other
Disease	Hirschsprung disease 1
Variation	info
Gene	RET
CLNDBN	Hirschsprung disease 1
Reversed	0
HGVS	NC_000010.10:g.43619231A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014947.2,