rs606231467

Orientation

plus

Stabilized

plus

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

Make rs606231467(A;A)

Make rs606231467(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

1

Position

156876128

Gene

NTRK1

is a	snp
is	mentioned by
dbSNP	rs606231467
dbSNP (classic)	rs606231467
ClinGen	rs606231467
ebi	rs606231467
HLI	rs606231467
Exac	rs606231467
Gnomad	rs606231467
Varsome	rs606231467
LitVar	rs606231467
Map	rs606231467
PheGenI	rs606231467
Biobank	rs606231467
1000 genomes	rs606231467
hgdp	rs606231467
ensembl	rs606231467
geneview	rs606231467
scholar	rs606231467
google	rs606231467
pharmgkb	rs606231467
gwascentral	rs606231467
openSNP	rs606231467
23andMe	rs606231467
SNPshot	rs606231467
SNPdbe	rs606231467
MSV3d	rs606231467
GWAS Ctlg	rs606231467

Max Magnitude

0

ClinVar
Risk	rs606231467(A;A)
Alt	rs606231467(A;A)
Reference	Rs606231467(G;G)
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.156845920G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000148946.3,