This variant maps to 2 locations

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

HGVS name

None

About this variant

This variant has 2506 sample genotypes, is associated with 10 phenotypes and is mentioned in 1 citation.

Variant displays