This variation has been flagged

Variation has more than 3 different alleles

Original source

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

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

Chromosome 17:72124177 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM941298

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

Variation displays