Original source

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

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

Chromosome 7:44147678 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930304, CM920307

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 22 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays