Original source

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

TTG/- | MAF: 0.29 (-)

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

Most severe consequence
Evidence status


Archive dbSNP rs146948708

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1093 individual genotypes.

Variation displays