This variant has been flagged

None of the variant alleles match the reference allele

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Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

This variant maps to 2 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs61200702

HGVS name

None

Genotyping chips

This variant has assays on: Illumina_Human660W-quad

About this variant

This variant overlaps 1 regulatory feature and has 2552 sample genotypes.

Variant displays