rs80236571

Orientation

plus

Stabilized

plus

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

Make rs80236571(A;A)

Make rs80236571(A;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43106497

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs80236571
dbSNP (classic)	rs80236571
ClinGen	rs80236571
ebi	rs80236571
HLI	rs80236571
Exac	rs80236571
Gnomad	rs80236571
Varsome	rs80236571
LitVar	rs80236571
Map	rs80236571
PheGenI	rs80236571
Biobank	rs80236571
1000 genomes	rs80236571
hgdp	rs80236571
ensembl	rs80236571
geneview	rs80236571
scholar	rs80236571
google	rs80236571
pharmgkb	rs80236571
gwascentral	rs80236571
openSNP	rs80236571
23andMe	rs80236571
SNPshot	rs80236571
SNPdbe	rs80236571
MSV3d	rs80236571
GWAS Ctlg	rs80236571

Max Magnitude

0

OMIM	164761
Desc
Variant	0022
Related	also

ClinVar
Risk	rs80236571(A;A)
Alt	rs80236571(A;A)
Reference	Rs80236571(G;G)
Significance	Other
Disease	Hirschsprung disease 1
Variation	info
Gene	RET
CLNDBN	Hirschsprung disease 1
Reversed	0
HGVS	NC_000010.10:g.43601945G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014951.2,