Marker Report

» Marker report for HGVM8134365

HGVbaseG2P Marker ID

HGVM8134365

Source database info

External marker ID rs7869402, imported from dbSNP

Variation type

SNP

Observed alleles

CCCCTGTACC(C):(T)TTCTCACTGC (IUPAC ambiguity code: Y) Show details..

Genomic location

Chr9:119,517,853 (view in genome browser: Ensembl | UCSC)

Marker status

This marker is currently ACTIVE (no revision history)

Cross-references

none

NINDS Parkinson's Disease (HGVST6) Show details..

Experiment title	Analysis method	Unadjusted p-value
Genotypic Association for Parkinson's Disease	Genotypic Association Additive Model (Parkinson's Disease)	not available
Genotypic Association for Parkinson's Disease	Genotypic Association (Parkinson's Disease)	not available

AREDS Age-related Macular Degeneration (AMD) (HGVST4) Show details..

Experiment title	Analysis method	Unadjusted p-value
Allelic Association for AMD Status (Illumina 100K)	Allelic Association (Illumina 100k)	not available

Ischemic Stroke Genetics Study (ISGS) (HGVST14) Show details..

Experiment title	Analysis method	Unadjusted p-value
Genotypic Association Ischemic Stroke Genetics Study (ISGS)	Genotypic Association in Additive model (ISGS)	not available

Other Frequency Data Using This Marker