Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs138700220

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2506 sample genotypes.

Variant displays