Original source

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

TTG/- | MAF: 0.25 (-)

Chromosome X:151398409-151398411 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs146948708

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2505 sample genotypes.

Variant displays