Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 19:41354331 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36204093

This variation has 4 HGVS names - click the plus to show

19:g.41354331C>T
ENST00000604123.4:c.142+16C>T
ENST00000604424.1:n.350+3129C>T
ENST00000539627.4:c.-30+3129C>T

About this variant

This variant overlaps 8 transcripts, has 1141 individual genotypes and is mentioned in 4 citations.

Variation displays