rs76764689

Orientation

plus

Stabilized

plus

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

Make rs76764689(C;T)

Make rs76764689(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

43100480

Gene

RET

is a	snp
is	mentioned by
dbSNP	rs76764689
dbSNP (classic)	rs76764689
ClinGen	rs76764689
ebi	rs76764689
HLI	rs76764689
Exac	rs76764689
Gnomad	rs76764689
Varsome	rs76764689
LitVar	rs76764689
Map	rs76764689
PheGenI	rs76764689
Biobank	rs76764689
1000 genomes	rs76764689
hgdp	rs76764689
ensembl	rs76764689
geneview	rs76764689
scholar	rs76764689
google	rs76764689
pharmgkb	rs76764689
gwascentral	rs76764689
openSNP	rs76764689
23andMe	rs76764689
SNPshot	rs76764689
SNPdbe	rs76764689
MSV3d	rs76764689
GWAS Ctlg	rs76764689

Max Magnitude

0

OMIM	164761
Desc
Variant	0018
Related	also

ClinVar
Risk	rs76764689(T;T)
Alt	rs76764689(T;T)
Reference	Rs76764689(C;C)
Significance	Other
Disease	Hirschsprung disease 1
Variation	info
Gene	RET
CLNDBN	Hirschsprung disease 1
Reversed	0
HGVS	NC_000010.10:g.43595928C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000014948.2,