Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.40 (T)
Location

Chromosome 7:128938247 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CS050392

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs2402939

This variation has 12 HGVS names - click the plus to show

7:g.128938247T>G
ENST00000489702.3:c.-12+413T>G
ENST00000613821.2:c.-12+198T>G
ENST00000249375.6:c.-12+2T>G
ENST00000488569.3:n.113+198T>G
ENST00000479582.3:c.-125+198T>G
ENST00000461416.1:n.69+198T>G
ENST00000473787.3:c.-12+198T>G
ENST00000357234.7:c.-12+198T>G
ENST00000402030.4:c.-12+198T>G
ENST00000464557.3:c.-158+198T>G
ENST00000477535.3:c.-12+198T>G

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays