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rs35669708

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs35669708(C;C)
Make rs35669708(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156881590
GeneNTRK1
is asnp
is mentioned by
dbSNPrs35669708
ebirs35669708
HLIrs35669708
Exacrs35669708
Varsomers35669708
Maprs35669708
PheGenIrs35669708
hapmaprs35669708
1000 genomesrs35669708
hgdprs35669708
ensemblrs35669708
gopubmedrs35669708
geneviewrs35669708
scholarrs35669708
googlers35669708
pharmgkbrs35669708
gwascentralrs35669708
openSNPrs35669708
23andMers35669708
23andMe allrs35669708
SNP Nexus

SNPshotrs35669708
SNPdbers35669708
MSV3drs35669708
GWAS Ctlgrs35669708
GMAF0.003673
Max Magnitude0
OMIM191315
Desc
Variant0004
Relatedalso


ClinVar
Risk rs35669708(A,C;A,C)
Alt rs35669708(A,C;A,C)
Reference rs35669708(G;G)
Significance Pathogenic
Disease not provided not specified Hereditary insensitivity to pain with anhidrosis
Variation info
Gene NTRK1
CLNDBN not provided not specified Hereditary insensitivity to pain with anhidrosis
Reversed 0
HGVS NC_000001.10:g.156851382G>A; NC_000001.10:g.156851382G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000224279.1, RCV000236228.1, RCV000013097.23,