rs606231466

Orientation

plus

Stabilized

plus

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

Make rs606231466(A;T)

Make rs606231466(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156868651

Gene

NTRK1

is a	snp
is	mentioned by
dbSNP	rs606231466
dbSNP (classic)	rs606231466
ClinGen	rs606231466
ebi	rs606231466
HLI	rs606231466
Exac	rs606231466
Gnomad	rs606231466
Varsome	rs606231466
LitVar	rs606231466
Map	rs606231466
PheGenI	rs606231466
Biobank	rs606231466
1000 genomes	rs606231466
hgdp	rs606231466
ensembl	rs606231466
geneview	rs606231466
scholar	rs606231466
google	rs606231466
pharmgkb	rs606231466
gwascentral	rs606231466
openSNP	rs606231466
23andMe	rs606231466
SNPshot	rs606231466
SNPdbe	rs606231466
MSV3d	rs606231466
GWAS Ctlg	rs606231466

Max Magnitude

0

ClinVar
Risk	rs606231466(T;T)
Alt	rs606231466(T;T)
Reference	Rs606231466(A;A)
Significance	Pathogenic
Disease	Hereditary insensitivity to pain with anhidrosis
Variation	info
Gene	NTRK1
CLNDBN	Hereditary insensitivity to pain with anhidrosis
Reversed	0
HGVS	NC_000001.10:g.156838443A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000148945.5,