This variation has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/A/C/G | Ancestral: C | Ambiguity code: N | MAF: < 0.01 (T)
Location

Chromosome X:49687616 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs56981136, rs17174087

This variation has 9 HGVS names - click the plus to show

Variation displays