Original source

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

Alleles
-/A | MAF: 0.42 (A)
Location

Chromosome X: between 151405273 and 151405274 (forward strand) | View in location tab

Most severe consequence

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1092 individual genotypes.

Variation displays