Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

AGTG/- | MAF: 0.37 (AGTG)

Chromosome X:136167098-136167101 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs143563921

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 23 transcripts and has 1100 individual genotypes.

Variation displays