Original source

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

Alleles
A/C | Ambiguity code: M
Location

Chromosome Y:9544033 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

Y:g.9544033A>C

About this variant

This variant overlaps 2 transcripts.

Variation displays