Original source

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

Alleles
-/TCTT/TTCT | MAF: 0.12 (-)
Location

Chromosome 22: between 36859193 and 36859194 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs138700220

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2506 individual genotypes.

Variation displays